Showing results (1841-1850 of 9,792) with videos related to
Sort By:
Pageof 980
American Journal of Human Genetics|December 7, 2014
Homozygous and compound-heterozygous mutations in TGDS cause Catel-Manzke syndromeNadja Ehmke, Almuth Caliebe, Rainer Koenig, et al.American Journal of Human Genetics|December 1, 2014
A rare functional noncoding variant at the GWAS-implicated MIR137/MIR2682 locus might confer risk to schizophrenia and bipolar disorderJubao Duan, Jianxin Shi, Alessia Fiorentino, et al.American Journal of Human Genetics|March 5, 2016
Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent MitophagySuzanne Lesage, Valérie Drouet, Elisa Majounie, et al.American Journal of Human Genetics|March 5, 2016
Disruption of POGZ Is Associated with Intellectual Disability and Autism Spectrum DisordersHolly A F Stessman, Marjolein H Willemsen, Michaela Fenckova, et al.American Journal of Human Genetics|December 3, 2015
Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic ArchitecturePhilip E Stuart, Rajan P Nair, Lam C Tsoi, et al.American Journal of Human Genetics|December 7, 2015
Mutations in Either TUBB or MAPRE2 Cause Circumferential Skin Creases Kunze TypeMala Isrie, Martin Breuss, Guoling Tian, et al.American Journal of Human Genetics|November 27, 2015
RTTN Mutations Cause Primary Microcephaly and Primordial Dwarfism in HumansHanan Shamseldin, Anas M Alazami, Melanie Manning, et al.American Journal of Human Genetics|October 3, 2015
Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk ScoresBjarni J Vilhjálmsson, Jian Yang, Hilary K Finucane, et al.American Journal of Human Genetics|October 23, 2013
Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive errorChing-Yu Cheng, Maria Schache, M Kamran Ikram, et al.American Journal of Human Genetics|October 1, 1989
Polymorphisms of the immunoglobulin heavy-chain delta gene and association with other constant-region genesJ C Benger, D W CoxPageof 980