| 0 | PI 561861 | OK91G109 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456833 | PI 561861 |
| 1 | PI 561862 | OK91G110 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456834 | PI 561862 |
| 2 | PI 561863 | OK91G111 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456835 | PI 561863 |
| 3 | PI 561864 | OK91G112 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456836 | PI 561864 |
| 4 | PI 561865 | OK91G113 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456837 | PI 561865 |
| 5 | PI 561866 | OK91G114 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456838 | PI 561866 |
| 6 | PI 561867 | OK91G115 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456839 | PI 561867 |
| 7 | PI 561868 | OK91G116 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456840 | PI 561868 |
| 8 | PI 561869 | OK91G117 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456841 | PI 561869 |
| 9 | PI 561870 | OK91G118 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456842 | PI 561870 |
| 10 | PI 561871 | OK91G119 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456843 | PI 561871 |
| 11 | PI 561872 | OK91G120 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456844 | PI 561872 |
| 12 | PI 561873 | OK91G121 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456845 | PI 561873 |
| 13 | PI 561874 | OK91G122 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456846 | PI 561874 |
| 14 | PI 561875 | OK91G123 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456847 | PI 561875 |
| 15 | PI 561876 | OK91G124 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456848 | PI 561876 |
| 16 | PI 561877 | OK91G125 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456849 | PI 561877 |
| 17 | PI 561878 | OK91G126 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456850 | PI 561878 |
| 18 | PI 561879 | OK91G127 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456851 | PI 561879 |
| 19 | PI 561880 | OK91G128 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456852 | PI 561880 |
| 20 | PI 561881 | OK91G129 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456853 | PI 561881 |
| 21 | PI 561882 | OK91G130 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456854 | PI 561882 |
| 22 | PI 561883 | OK91G131 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456855 | PI 561883 |
| 23 | PI 561884 | OK91G132 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456856 | PI 561884 |
| 24 | PI 561885 | OK91G133 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456857 | PI 561885 |
| 25 | PI 561886 | OK91G134 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456858 | PI 561886 |
| 26 | PI 561887 | OK91G135 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456859 | PI 561887 |
| 27 | PI 561888 | OK91G136 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456860 | PI 561888 |
| 28 | PI 561889 | OK91G137 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456861 | PI 561889 |
| 29 | PI 561890 | OK91G138 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456862 | PI 561890 |
| 30 | PI 561891 | OK91G139 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456863 | PI 561891 |
| 31 | PI 561892 | OK91G140 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456864 | PI 561892 |
| 32 | PI 561893 | OK91G141 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456865 | PI 561893 |
| 33 | PI 561894 | OK91G142 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456866 | PI 561894 |
| 34 | PI 561895 | OK91G143 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456867 | PI 561895 |
| 35 | PI 561896 | OK91G144 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456868 | PI 561896 |
| 36 | PI 561897 | OK91G145 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456869 | PI 561897 |
| 37 | PI 561898 | OK91G146 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456870 | PI 561898 |
| 38 | PI 561899 | OK91G147 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456871 | PI 561899 |
| 39 | PI 561900 | OK91G148 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456872 | PI 561900 |
| 40 | PI 561901 | OK91G149 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456873 | PI 561901 |
| 41 | PI 561902 | OK91G150 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456874 | PI 561902 |
| 42 | PI 561903 | OK91G151 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456875 | PI 561903 |
| 43 | PI 561904 | OK91G152 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456876 | PI 561904 |
| 44 | PI 561905 | OK91G153 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456877 | PI 561905 |
| 45 | PI 561906 | OK91G154 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456878 | PI 561906 |
| 46 | PI 561907 | OK91G155 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456879 | PI 561907 |
| 47 | PI 561908 | OK91G156 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456880 | PI 561908 |
| 48 | PI 561909 | OK91G157 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456881 | PI 561909 |
| 49 | PI 561910 | OK91G158 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456882 | PI 561910 |
| 50 | PI 561911 | OK91G159 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456883 | PI 561911 |
| 51 | PI 561912 | OK91G160 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456884 | PI 561912 |
| 52 | PI 561913 | OK91G161 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456885 | PI 561913 |
| 53 | PI 561914 | OK91G162 | Triticum aestivum L. subsp. aestivum | Oklahoma, United States | NSGC |  | | 1992 | DEVELOPED | 1992 | | | | | Genetic material | Pairs of near-isolines differing for the presence or absence of 1RS.1BL were developed by selfing heterozygous plants (1RS.1BL//1B) in the F2 to F4 generations. One pair of homozygous near-isolines was isolated in each of 27 F5 families descending from a different F2 plant. No selection was imposed except for chromosome type. Segregation has been observed for plant stature (mostly semi-dwarf, some dwarf), and reaction to soil-born mosaic virus and tan spot (Pyrenophora tritici-repentis). This variation is not linked to chromosome type 1B or 1RS.1BL. [See PI 561861-561914 for accessions from the same Crop Science registration.] | 1456886 | PI 561914 |