Showing results (5701-5710 of 7,441) with videos related to
Sort By:
Pageof 745
Nature Genetics|July 19, 2022
Reference genome assemblies reveal the origin and evolution of allohexaploid oatYuanying Peng, Honghai Yan, Laichun Guo, et al.Nature Genetics|August 1, 1994
A physical map and candidate genes in the BRCA1 region on chromosome 17q12-21H M Albertsen, S A Smith, S Mazoyer, et al.Nature Genetics|August 1, 1994
Identification of novel genes, SYT and SSX, involved in the t(X;18)(p11.2;q11.2) translocation found in human synovial sarcomaJ Clark, P J Rocques, A J Crew, et al.Nature Genetics|August 1, 1994
Studying human mutations by sperm typing: instability of CAG trinucleotide repeats in the human androgen receptor geneL Zhang, E P Leeflang, J Yu, et al.Nature Genetics|September 1, 1994
Neomorphic agouti mutations in obese yellow miceD M Duhl, H Vrieling, K A Miller, et al.Nature Genetics|September 1, 1994
An autosomal locus causing autoimmune disease: autoimmune polyglandular disease type I assigned to chromosome 21J Aaltonen, P Björses, L Sandkuijl, et al.Nature Genetics|September 1, 1994
Length of uninterrupted CGG repeats determines instability in the FMR1 geneE E Eichler, J J Holden, B W Popovich, et al.Nature Genetics|April 1, 1993
Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita)A L George, M A Crackower, J A Abdalla, et al.Nature Genetics|April 1, 1993
Clustered base substitutions in CTP synthetase conferring drug resistance in Chinese hamster ovary cellsJ Whelan, G Phear, M Yamauchi, et al.Nature Genetics|April 1, 1993
Kniest and Stickler dysplasia phenotypes caused by collagen type II gene (COL2A1) defectA Winterpacht, M Hilbert, U Schwarze, et al.Pageof 745