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American Journal of Human Genetics|October 1, 1988
Molecular and cytogenetic characterization of a de novo t(5p;21q) in a patient previously diagnosed as monosomy 21M C Phelan, C C Morton, R E Stevenson, et al.American Journal of Human Genetics|October 1, 1988
Genetic studies on the Senegal population. I. Mitochondrial DNA polymorphismsR Scozzari, A Torroni, O Semino, et al.American Journal of Human Genetics|August 1, 2017
Continuity and Admixture in the Last Five Millennia of Levantine History from Ancient Canaanite and Present-Day Lebanese Genome SequencesMarc Haber, Claude Doumet-Serhal, Christiana Scheib, et al.American Journal of Human Genetics|August 22, 2017
Homozygous Mutations in TBC1D23 Lead to a Non-degenerative Form of Pontocerebellar HypoplasiaIsaac Marin-Valencia, Andreas Gerondopoulos, Maha S Zaki, et al.American Journal of Human Genetics|August 22, 2017
Homozygous Truncating Variants in TBC1D23 Cause Pontocerebellar Hypoplasia and Alter Cortical DevelopmentEkaterina L Ivanova, Frédéric Tran Mau-Them, Saima Riazuddin, et al.American Journal of Human Genetics|October 1, 1987
An XXX male resulting from paternal X-Y interchange and maternal X-X nondisjunctionG Annerén, M Andersson, D C Page, et al.American Journal of Human Genetics|June 28, 2016
Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell TraitsNathalie Chami, Ming-Huei Chen, Andrew J Slater, et al.American Journal of Human Genetics|June 21, 2016
Trans-ethnic Meta-analysis and Functional Annotation Illuminates the Genetic Architecture of Fasting Glucose and InsulinChing-Ti Liu, Sridharan Raghavan, Nisa Maruthur, et al.American Journal of Human Genetics|July 18, 2017
CRISPR/Cas9-Mediated Scanning for Regulatory Elements Required for HPRT1 Expression via Thousands of Large, Programmed Genomic DeletionsMolly Gasperini, Gregory M Findlay, Aaron McKenna, et al.American Journal of Human Genetics|April 1, 1989
Estimating the power of a proposed linkage study for a complex genetic traitL M Ploughman, M BoehnkePageof 979