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American Journal of Human Genetics|October 4, 2014
Cryptic and complex chromosomal aberrations in early-onset neuropsychiatric disordersHarrison Brand, Vamsee Pillalamarri, Ryan L Collins, et al.American Journal of Human Genetics|January 1, 1989
A simple method to detect and estimate heterogeneity: application to Huntington disease, diabetes, and HIV seroconversionH PayamiAmerican Journal of Human Genetics|March 1, 1989
Branching enzyme activity of cultured amniocytes and chorionic villi: prenatal testing for type IV glycogen storage diseaseB I Brown, D H BrownAmerican Journal of Human Genetics|March 1, 1989
Evidence from family studies that the gene causing Huntington disease is telomeric to D4S95 and D4S90C Robbins, J Theilmann, S Youngman, et al.American Journal of Human Genetics|October 14, 2014
Structural architecture of SNP effects on complex traitsEric R Gamazon, Nancy J Cox, Lea K DavisAmerican Journal of Human Genetics|September 6, 2014
Mutations in FEZF1 cause Kallmann syndromeL Damla Kotan, B Ian Hutchins, Yusuf Ozkan, et al.American Journal of Human Genetics|September 6, 2014
Synaptotagmin 2 mutations cause an autosomal-dominant form of lambert-eaton myasthenic syndrome and nonprogressive motor neuropathyDavid N Herrmann, Rita Horvath, Janet E Sowden, et al.American Journal of Human Genetics|June 4, 2013
Genome-wide characterization of shared and distinct genetic components that influence blood lipid levels in ethnically diverse human populationsMarc A Coram, Qing Duan, Thomas J Hoffmann, et al.American Journal of Human Genetics|August 1, 1990
Friedreich ataxia in Italian families: genetic homogeneity and linkage disequilibrium with the marker loci D9S5 and D9S15M Pandolfo, G Sirugo, A Antonelli, et al.American Journal of Human Genetics|August 1, 1990
Joint estimation of recombination fractions and interference coefficients in multilocus linkage analysisL P Zhao, E Thompson, R PrenticePageof 980