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American Journal of Human Genetics|April 2, 2019
Bi-allelic Mutations in TTC21A Induce Asthenoteratospermia in Humans and MiceWangjie Liu, Xiaojin He, Shenmin Yang, et al.American Journal of Human Genetics|April 2, 2019
Diagnostic Utility of Genome-wide DNA Methylation Testing in Genetically Unsolved Individuals with Suspected Hereditary ConditionsErfan Aref-Eshghi, Eric G Bend, Samantha Colaiacovo, et al.American Journal of Human Genetics|April 2, 2019
Genetic Architectures of Childhood- and Adult-Onset Asthma Are Partly DistinctManuel A R Ferreira, Riddhima Mathur, Judith M Vonk, et al.American Journal of Human Genetics|April 2, 2019
De Novo and Inherited Pathogenic Variants in KDM3B Cause Intellectual Disability, Short Stature, and Facial DysmorphismIllja J Diets, Roos van der Donk, Kristina Baltrunaite, et al.American Journal of Human Genetics|August 1, 1987
Y chromosome--specific DNA sequences in Turner-syndrome mosaicismR M Gemmill, L Pearce-Birge, H Bixenman, et al.American Journal of Human Genetics|August 1, 1987
A study of 609 HLA haplotypes marking for the hemochromatosis gene: (1) mapping of the gene near the HLA-A locus and characters required to define a heterozygous population and (2) hypothesis concerning the underlying cause of hemochromatosis-HLA associationM Simon, L Le Mignon, R Fauchet, et al.American Journal of Human Genetics|July 1, 1987
Mapping the Wilson disease locus to a cluster of linked polymorphic markers on chromosome 13A M Bowcock, L A Farrer, L L Cavalli-Sforza, et al.American Journal of Human Genetics|June 1, 1988
Segregation analysis with uncertain ascertainment: application to Fanconi anemiaA Rogatko, A D AuerbachAmerican Journal of Human Genetics|March 1, 1990
Genotype assignment in Gaucher disease by selective amplification of the active glucocerebrosidase geneN Firon, N Eyal, E H Kolodny, et al.American Journal of Human Genetics|March 1, 1990
Determination of Y chromosome aneuploidy in human sperm nuclei by nonradioactive in situ hybridizationM Guttenbach, M SchmidPageof 979