Zobrazeno 1 - 3
of 3
pro vyhledávání: '"G. D. Raymer"'
Publikováno v:
Journal of Heredity. 84:466-474
Heterozygotes for cleidocranial dysplasia (Ccd) and short digits (Dsh) were crossed to test whether synergistic interactions occur between different dominant mutations whose individual pleiotropic phenotypic effects exhibit a common feature. These un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7674a3bc3ecabf6de49b97fd04bdc614
https://doi.org/10.1093/oxfordjournals.jhered.a111373
https://doi.org/10.1093/oxfordjournals.jhered.a111373
Publikováno v:
Genetics. 100:427-453
Thirty-four independent nonviable c-locus mutations (types cal, albino lethal and cas, albino subvital), derived from radiation experiments, were tested for involvement of nearby markers tp, Mod-2, sh-1, and Hbb: 10, 22, and 2 involved, respectively,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6115892a6b4fe01836cc0d939b68f0da
https://doi.org/10.1093/genetics/100.3.427
https://doi.org/10.1093/genetics/100.3.427
Autor:
G. D. Raymer, Liane B. Russell
Publikováno v:
Genetics. 92(1)
The stage at which homozygotes die was determined for 28 mutations (general symbol c*) at the albino (c) locus, of which 26 had earlier been found to be probably prenatally lethal. Within each of the mutant stocks, the uterine contents of c*/cch fema
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::232a155438b27622073153992d2f58b7
https://pubmed.ncbi.nlm.nih.gov/574104
https://pubmed.ncbi.nlm.nih.gov/574104