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American Journal of Human Genetics|November 26, 2013
Integrating GWASs and human protein interaction networks identifies a gene subnetwork underlying alcohol dependenceShizhong Han, Bao-Zhu Yang, Henry R Kranzler, et al.American Journal of Human Genetics|July 5, 2014
Aicardi-Goutières syndrome is caused by IFIH1 mutationsHirotsugu Oda, Kenji Nakagawa, Junya Abe, et al.American Journal of Human Genetics|September 15, 2015
Penetrance of Hemochromatosis in HFE Genotypes Resulting in p.Cys282Tyr and p.[Cys282Tyr];[His63Asp] in the eMERGE NetworkCarlos J Gallego, Amber Burt, Agnes S Sundaresan, et al.American Journal of Human Genetics|May 31, 2016
Genomic Profiling of Thyroid Cancer Reveals a Role for Thyroglobulin in MetastasisAbdul K Siraj, Tariq Masoodi, Rong Bu, et al.American Journal of Human Genetics|May 31, 2016
RNA Interference Prevents Autosomal-Dominant Hearing LossSeiji B Shibata, Paul T Ranum, Hideaki Moteki, et al.American Journal of Human Genetics|May 1, 1989
The probability of detecting the origin of nondisjunction of autosomal trisomiesA ChakravartiAmerican Journal of Human Genetics|May 1, 1989
Analysis of liver/bone/kidney alkaline phosphatase mRNA, DNA, and enzymatic activity in cultured skin fibroblasts from 14 unrelated patients with severe hypophosphatasiaM J Weiss, K Ray, M D Fallon, et al.American Journal of Human Genetics|April 9, 2016
Biallelic Mutations in PDE10A Lead to Loss of Striatal PDE10A and a Hyperkinetic Movement Disorder with Onset in InfancyChristine P Diggle, Stacey J Sukoff Rizzo, Michael Popiolek, et al.American Journal of Human Genetics|April 12, 2016
Biallelic Mutations in GNB3 Cause a Unique Form of Autosomal-Recessive Congenital Stationary Night BlindnessAjoy Vincent, Isabelle Audo, Erika Tavares, et al.American Journal of Human Genetics|June 4, 2016
Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain DeficiencyRikke K J Olsen, Eliška Koňaříková, Teresa A Giancaspero, et al.Pageof 979