Showing results (1411-1420 of 9,792) with videos related to
Sort By:
Pageof 980
American Journal of Human Genetics|October 11, 2001
Large upward bias in estimation of locus-specific effects from genomewide scansH H Göring, J D Terwilliger, J BlangeroAmerican Journal of Human Genetics|July 27, 2001
MYO6, the human homologue of the gene responsible for deafness in Snell's waltzer mice, is mutated in autosomal dominant nonsyndromic hearing lossS Melchionda, N Ahituv, L Bisceglia, et al.American Journal of Human Genetics|August 14, 2001
MC1R genotype modifies risk of melanoma in families segregating CDKN2A mutationsN F Box, D L Duffy, W Chen, et al.American Journal of Human Genetics|August 2, 2001
Studies of association between the gene for calpain-10 and type 2 diabetes mellitus in the United KingdomJ C Evans, T M Frayling, P G Cassell, et al.American Journal of Human Genetics|November 15, 2000
Identification of a locus for autosomal dominant polycystic liver disease, on chromosome 19p13.2-13.1D M Reynolds, C T Falk, A Li, et al.American Journal of Human Genetics|September 14, 2000
A mutation in the rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in malesI Meloni, M Bruttini, I Longo, et al.American Journal of Human Genetics|October 18, 2000
A locus for autosomal dominant colobomatous microphthalmia maps to chromosome 15q12-q15L Morlé, M Bozon, J C Zech, et al.American Journal of Human Genetics|November 4, 2000
Parental attitudes toward genetic testing for pediatric deafnessJ W Brunger, G S Murray, M O'Riordan, et al.American Journal of Human Genetics|November 9, 2000
Primary autosomal recessive microcephaly: MCPH5 maps to 1q25-q32C R Jamieson, J P Fryns, J Jacobs, et al.Pageof 980