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American Journal of Human Genetics|November 1, 1989
Testing separate families of segregation hypotheses: bootstrap methodsN Schork, M A SchorkAmerican Journal of Human Genetics|December 27, 2016
A Syndromic Neurodevelopmental Disorder Caused by De Novo Variants in EBF3Hsiao-Tuan Chao, Mariska Davids, Elizabeth Burke, et al.American Journal of Human Genetics|January 10, 2017
The Genetic Architecture of Gene Expression in Peripheral BloodLuke R Lloyd-Jones, Alexander Holloway, Allan McRae, et al.American Journal of Human Genetics|September 1, 1991
Genetic mapping of the beta 1 GABA receptor gene to human chromosome 4, using a tetranucleotide repeat polymorphismM Dean, S Lucas-Derse, A Bolos, et al.American Journal of Human Genetics|September 1, 1991
A unique mutation in the vitamin D receptor gene in three Japanese patients with vitamin D-dependent rickets type II: utility of single-strand conformation polymorphism analysis for heterozygous carrier detectionT Saijo, M Ito, E Takeda, et al.American Journal of Human Genetics|February 12, 2002
Bias in estimates of quantitative-trait-locus effect in genome scans: demonstration of the phenomenon and a method-of-moments procedure for reducing biasDavid B Allison, Jose R Fernandez, Moonseong Heo, et al.American Journal of Human Genetics|March 15, 2006
A fine-scale linkage-disequilibrium measure based on length of haplotype sharingYan Wang, Lue Ping Zhao, Sandrine DudoitAmerican Journal of Human Genetics|March 15, 2006
Uroporphyrinogen III synthase knock-in mice have the human congenital erythropoietic porphyria phenotype, including the characteristic light-induced cutaneous lesionsDavid F Bishop, Annika Johansson, Robert Phelps, et al.American Journal of Human Genetics|March 15, 2006
A novel primary immunodeficiency with specific natural-killer cell deficiency maps to the centromeric region of chromosome 8Celine Eidenschenk, Jean Dunne, Emmanuelle Jouanguy, et al.American Journal of Human Genetics|June 1, 1989
Human pregnancy-specific beta 1-glycoproteins are coded within chromosome 19T R Barnett, W Pickle, P M Rae, et al.Pageof 979