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American Journal of Human Genetics|December 29, 2005
Identification of an X-chromosomal locus and haplotype modulating the phenotype of a mitochondrial DNA disorderGavin Hudson, Sharon Keers, Patrick Yu-Wai-Man, et al.
American Journal of Human Genetics|May 1, 1991
Atopic disease and immunoglobulin E in twins reared apart and togetherB Hanson, M McGue, B Roitman-Johnson, et al.
American Journal of Human Genetics|May 1, 1991
Testing for association between disease and linked marker loci: a log-linear-model analysisL Tiret, P Amouyel, R Rakotovao, et al.
American Journal of Human Genetics|September 13, 2016
NAXE Mutations Disrupt the Cellular NAD(P)HX Repair System and Cause a Lethal Neurometabolic Disorder of Early ChildhoodLaura S Kremer, Katharina Danhauser, Diran Herebian, et al.
American Journal of Human Genetics|September 13, 2016
GWIS: Genome-Wide Inferred Statistics for Functions of Multiple PhenotypesHarold A Nieuwboer, René Pool, Conor V Dolan, et al.
American Journal of Human Genetics|September 3, 2016
Complex Sources of Variation in Tissue Expression Data: Analysis of the GTEx Lung TranscriptomeMatthew N McCall, Peter B Illei, Marc K Halushka
American Journal of Human Genetics|September 3, 2016
Trans-ethnic Fine Mapping Highlights Kidney-Function Genes Linked to Salt SensitivityAnubha Mahajan, Aylin R Rodan, Thu H Le, et al.
American Journal of Human Genetics|August 30, 2016
Impaired Presynaptic High-Affinity Choline Transporter Causes a Congenital Myasthenic Syndrome with Episodic ApneaStéphanie Bauché, Seana O'Regan, Yoshiteru Azuma, et al.
American Journal of Human Genetics|August 1, 1989
Analyzing the relationship between age at onset and risk to relativesM C Neale, L J Eaves, J K Hewitt, et al.
American Journal of Human Genetics|May 30, 2017
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric TraitsIoanna Tachmazidou, Dániel Süveges, Josine L Min, et al.
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