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Human Genetics|January 1, 1995
PKU in Slovakia: mutation screening and haplotype analysisL Kádasi, H Poláková, E Feráková, et al.Human Genetics|January 1, 1995
Trisomy 21 and maternal age of menopause: does reproductive age rather than chronological age influence risk of nondisjunction?O P Phillips, S Cromwell, M Rivas, et al.Human Genetics|January 1, 1995
Positional cloning of cDNAs from the human chromosome 3p21-22 region identifies a clustered organization of zinc-finger genesV Calabrò, G Pengue, P C Bartoli, et al.Human Genetics|October 1, 1993
An unreported RFLP for probe 218 EP6 that is useful in linkage analysis of adult polycystic kidney diseaseS Jeffery, S MorganHuman Genetics|March 1, 1994
Isolation and mapping of cosmid markers on human chromosome 22, including one within the submicroscopically deleted region of DiGeorge syndromeH Kurahashi, K Akagi, K Karakawa, et al.Human Genetics|April 1, 1994
A Sau3A polymorphism in the 5' end of the IT15 gene that nonrandomly segregates with the Huntington disease trinucleotide expansionL Carlock, K Gutridge, T VoHuman Genetics|April 1, 1994
PstI identifies biallelic DNA polymorphism of the human casein kinase 2 alpha gene (CSNK2A1)S Singh, I Jantke, M Simon, et al.Human Genetics|March 1, 1995
Identifying chromosomal fragile sites from individuals: a multinomial statistical modelU Böhm, P F Dahm, B F McAllister, et al.Human Genetics|March 1, 1995
Chromosomal localization of the human NF-E2 family of bZIP transcription factors by fluorescence in situ hybridizationJ Y Chan, M C Cheung, P Moi, et al.Human Genetics|March 1, 1995
Somatic expansion of the (CAG)n repeat in Huntington disease brainsK E De Rooij, P A De Koning Gans, R A Roos, et al.Pageof 958