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American Journal of Human Genetics|August 14, 2012
TCTN3 mutations cause Mohr-Majewski syndromeSophie Thomas, Marine Legendre, Sophie Saunier, et al.American Journal of Human Genetics|August 14, 2012
RBPJ mutations identified in two families affected by Adams-Oliver syndromeSusan J Hassed, Graham B Wiley, Shaofeng Wang, et al.American Journal of Human Genetics|February 1, 1990
The power of identity-by-state methods for linkage analysisD T Bishop, J A WilliamsonAmerican Journal of Human Genetics|February 1, 1990
DNA fingerprinting for forensic identification: potential effects on data interpretation of subpopulation heterogeneity and band number variabilityJ E CohenAmerican Journal of Human Genetics|October 9, 2012
Population genetic inference from personal genome data: impact of ancestry and admixture on human genomic variationJeffrey M Kidd, Simon Gravel, Jake Byrnes, et al.American Journal of Human Genetics|October 9, 2012
Mutations in calmodulin cause ventricular tachycardia and sudden cardiac deathMette Nyegaard, Michael T Overgaard, Mads T Søndergaard, et al.American Journal of Human Genetics|September 18, 2012
A population-based study of autosomal-recessive disease-causing mutations in a founder populationJessica X Chong, Rebecca Ouwenga, Rebecca L Anderson, et al.American Journal of Human Genetics|October 2, 2012
Estimating genetic effects and quantifying missing heritability explained by identified rare-variant associationsDajiang J Liu, Suzanne M LealAmerican Journal of Human Genetics|August 28, 2012
Mutation of membrane type-1 metalloproteinase, MT1-MMP, causes the multicentric osteolysis and arthritis disease Winchester syndromeBrad R Evans, Rebecca A Mosig, Mollie Lobl, et al.American Journal of Human Genetics|July 4, 2012
A homozygous mutation in KCTD7 links neuronal ceroid lipofuscinosis to the ubiquitin-proteasome systemJohn F Staropoli, Amel Karaa, Elaine T Lim, et al.Pageof 979