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American Journal of Human Genetics|November 25, 2000
The phylogeography of Brazilian Y-chromosome lineagesD R Carvalho-Silva, F R Santos, J Rocha, et al.American Journal of Human Genetics|December 15, 2000
Mutation analysis of the entire PKD1 gene: genetic and diagnostic implicationsS Rossetti, L Strmecki, V Gamble, et al.American Journal of Human Genetics|March 26, 1999
Germ-line mosaicism in tuberous sclerosis: how common?V M Rose, K S Au, G Pollom, et al.American Journal of Human Genetics|March 26, 1999
Mutations in a dominant-negative isoform correlate with phenotype in inherited cardiac arrhythmiasR Mohammad-Panah, S Demolombe, N Neyroud, et al.American Journal of Human Genetics|March 26, 1999
The 2588G-->C mutation in the ABCR gene is a mild frequent founder mutation in the Western European population and allows the classification of ABCR mutations in patients with Stargardt diseaseA Maugeri, M A van Driel, D J van de Pol, et al.American Journal of Human Genetics|March 26, 1999
Genetic linkage of IgA deficiency to the major histocompatibility complex: evidence for allele segregation distortion, parent-of-origin penetrance differences, and the role of anti-IgA antibodies in disease predispositionI Vorechovský, A D Webster, A Plebani, et al.American Journal of Human Genetics|March 26, 1999
Precise genetic mapping and haplotype analysis of the familial dysautonomia gene on human chromosome 9q31A Blumenfeld, S A Slaugenhaupt, C B Liebert, et al.American Journal of Human Genetics|March 26, 1999
A note on power approximations for the transmission/disequilibrium testM KnappAmerican Journal of Human Genetics|August 5, 2000
Inactivation of germline mutant APC alleles by attenuated somatic mutations: a molecular genetic mechanism for attenuated familial adenomatous polyposisL K Su, C J Barnes, W Yao, et al.American Journal of Human Genetics|June 28, 2000
SNPing away at complex diseases: analysis of single-nucleotide polymorphisms around APOE in Alzheimer diseaseE R Martin, E H Lai, J R Gilbert, et al.Pageof 979