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American Journal of Human Genetics|July 11, 2006
A geographically explicit genetic model of worldwide human-settlement historyHua Liu, Franck Prugnolle, Andrea Manica, et al.American Journal of Human Genetics|July 11, 2006
Mutation in TRMU related to transfer RNA modification modulates the phenotypic expression of the deafness-associated mitochondrial 12S ribosomal RNA mutationsMin-Xin Guan, Qingfeng Yan, Xiaoming Li, et al.American Journal of Human Genetics|July 11, 2006
A coalescence-guided hierarchical Bayesian method for haplotype inferenceYu Zhang, Tianhua Niu, Jun S LiuAmerican Journal of Human Genetics|July 11, 2006
Mutations in the novel mitochondrial protein REEP1 cause hereditary spastic paraplegia type 31Stephan Züchner, Gaofeng Wang, Khanh-Nhat Tran-Viet, et al.American Journal of Human Genetics|July 11, 2006
Loss-of-function mutations in euchromatin histone methyl transferase 1 (EHMT1) cause the 9q34 subtelomeric deletion syndromeTjitske Kleefstra, Han G Brunner, Jeanne Amiel, et al.American Journal of Human Genetics|May 1, 1991
Extended haplotypes and linkage disequilibrium between 11 markers at the APOA1-C3-A4 gene cluster on chromosome 11P Benlian, C Boileau, N Loux, et al.American Journal of Human Genetics|May 1, 1991
A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination ratesK H Buetow, R Shiang, P Yang, et al.American Journal of Human Genetics|May 1, 1991
2,8-Dihydroxyadenine lithiasis in a Japanese patient heterozygous at the adenine phosphoribosyltransferase locusA Sahota, J Chen, M A Behzadian, et al.American Journal of Human Genetics|May 30, 2020
Non-parametric Polygenic Risk Prediction via Partitioned GWAS Summary StatisticsSung Chun, Maxim Imakaev, Daniel Hui, et al.American Journal of Human Genetics|May 30, 2020
Loss of Function of RIMS2 Causes a Syndromic Congenital Cone-Rod Synaptic Disease with Neurodevelopmental and Pancreatic InvolvementSabrina Mechaussier, Basamat Almoallem, Christina Zeitz, et al.Pageof 979