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Annals of Human Genetics|October 6, 1998
A splicing mutation of the RHAG gene associated with the Rhnull phenotypeM Kawano, S Iwamoto, H Okuda, et al.Annals of Human Genetics|October 6, 1998
Hidden linkage: a comparison of the affected sib pair (ASP) test and transmission/disequilibrium test (TDT)R E McGinnisAnnals of Human Genetics|October 6, 1998
Characterization of polymorphisms at the 11 beta-hydroxylase (CYP11B1) locusC A Skinner, N Yousaf, J W Honour, et al.Annals of Human Genetics|May 8, 2008
On the origin of the transthyretin Val30Met familial amyloid polyneuropathyC Zaros, E Genin, U Hellman, et al.Annals of Human Genetics|May 8, 2008
Genetic epidemiology of subclinical cardiovascular disease in the diabetes heart studyD W Bowden, A B Lehtinen, J T Ziegler, et al.Annals of Human Genetics|May 8, 2008
Correlation analyses reveal a substantial influence of allelic gaps on the investigation of genetic diversity of modern human populations with microsatellitesS Guha, R ChakrabortyAnnals of Human Genetics|October 1, 1991
The gene for human neurone specific ubiquitin C-terminal hydrolase (UCHL1, PGP9.5) maps to chromosome 4p14Y H Edwards, M F Fox, S Povey, et al.Annals of Human Genetics|December 21, 2007
Association of polymorphic sites in the OCA2 gene with eye colour using the tree scanning methodW Branicki, U Brudnik, T Kupiec, et al.Annals of Human Genetics|December 21, 2007
Testing for equality of standardized composite measures of linkage disequilibriumD C Hamilton, D E C ColeAnnals of Human Genetics|February 11, 2014
A DFNA5 mutation identified in Japanese families with autosomal dominant hereditary hearing lossAyako Nishio, Yoshihiro Noguchi, Tatsuya Sato, et al.Pageof 231