| scholarly article | Q13442814 |
| P50 | author | Charles Edmund Ford | Q23612252 |
| P2093 | author name string | A. G. Searle | |
| C. V. Beechey | |||
| P2860 | cites work | A comparison of the mutagenic effectiveness of chronic neutron- and gamma-irradiation of mouse spermatogonia | Q72909162 |
| A RECIPROCAL TRANSLOCATION IN THE MOUSE BETWEEN THE X CHROMOSOME AND A SHORT AUTOSOME | Q77161985 | ||
| Mammalian pachytene chromosome mapping and somatic chromosome identification | Q78857313 | ||
| Genetic analysis of induced deletions and of spontaneous nondisjunction involving chromosome 2 of the mouse | Q79006834 | ||
| A preliminary pachytene chromosome map of the house mouse | Q87309231 | ||
| Affinity: A New Genetic Phenomenon in the House Mouse: Evidence from Distant Crosses | Q59088580 | ||
| Differential transmission of translocations induced in spermatogonia of mice by irradiation | Q71273668 | ||
| Muted, a new mutant affecting coat colour and otoliths of the mouse, and its position in linkage group XIV | Q71279260 | ||
| Producing and detecting paracentric chromosomal inversions in mice | Q71786847 | ||
| The positions of the centromeres in linkage groups II and IX of the mouse | Q72040441 | ||
| Sex differences in recombination of linked genes in animals | Q72264586 | ||
| Reciprocal translocations | Q72383402 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | genetics | Q7162 |
| chromosome abnormality | Q744962 | ||
| P304 | page(s) | 215-235 | |
| P577 | publication date | 1971-10-01 | |
| P1433 | published in | Genetics Research | Q15758859 |
| P1476 | title | Meiotic disjunction in mouse translocations and the determination of centromere position | |
| P478 | volume | 18 |
| Q48678528 | A candidate model for Angelman syndrome in the mouse |
| Q67429723 | A genetic method for measuring non-disjunction in mice with Robertsonian translocations |
| Q24796252 | An application of molecular genotyping in mice |
| Q33963189 | Assignment of genes to regions of mouse chromosomes |
| Q41073929 | Chromosomal abnormalities and the morphology of mouse sperm heads |
| Q41052635 | Chromosomal radiosensitivity and karyotype in mice using cultured peripheral blood lymphocytes, and comparison with this system in man |
| Q41456919 | Chromosome segregation at meiosis I in female T(2;4)1Gö/+ mice: no evidence for a decreased crossover frequency with maternal age. |
| Q69219611 | Do the H-2 and T-Loci of the Mouse have a Function in the Haploid Phase of Sperm ? |
| Q67265542 | Double translocation t(7;12),t(2;6) heterozygosity in one family. A contribution to the trisomy 12p syndrome |
| Q55052972 | Embryological and molecular investigations of parental imprinting on mouse chromosome 7. |
| Q56049804 | Factors affecting the observed number of young resulting from adjacent-2 disjunction in mice carrying a translocation |
| Q27316512 | Gene Dosage Effects at the Imprinted Gnas Cluster |
| Q68650344 | Genome imprinting phenomena on mouse chromosome 7 |
| Q69440247 | Genomic imprinting: normal complementation of murine chromosome 16 |
| Q68289334 | Male meiotic behaviour and male and female litter size in mice with the T(2;8)26H and T(1;13)70H reciprocal translocations |
| Q45138573 | Meiotic disjunction, sex-determination and embryonic lethality in an X-linked "simple" translocation of the onion fly, Hylemya antiqua (Meigen). |
| Q44036292 | Mouse chromosome 1. |
| Q40114078 | Nondisjunction |
| Q33965893 | Nondisjunction rates and abnormal embryonic development in a mouse cross between heterozygotes carrying a (7, 18) robertsonian translocation chromosome |
| Q68296324 | Parental age and recombination frequency in the house mouse |
| Q35134051 | Proximal chiasma localization within an interstitial chromosome segment, a likely correlate of adjacent-2 segregation of translocation causing multivalents in the mouse |
| Q33988267 | Quinacrine fluorescent chromosome analysis of the Snell translocation in the mouse |
| Q33990323 | Reciprocal translocations and translocation disomics of aspergillus and their use for genetic mapping |
| Q64929446 | Technical advances contribute to the study of genomic imprinting. |
| Q39628697 | The Cytogenetics of Neurospora |
| Q70763083 | The Splotch (Sp1H) and Splotch-delayed (Spd) alleles: differential phenotypic effects on neural crest and limb musculature |
| Q33988260 | The T6 translocation in the mouse: its use in trisomy mapping, centromere localization, and cytological identification of linkage group 3 |
| Q73208039 | The mouse chromosome 7 distal imprinting domain maps to G-bands F4/F5 |
| Q39622271 | The spermatozoan genome and fertility |
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