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American Journal of Human Genetics|May 23, 2002
A second locus for very-late-onset Alzheimer disease: a genome scan reveals linkage to 20p and epistasis between 20p and the amyloid precursor protein regionJane M Olson, Katrina A B Goddard, Doreen M DudekAmerican Journal of Human Genetics|June 7, 2000
Split-hand/split-foot malformation is caused by mutations in the p63 gene on 3q27P Ianakiev, M W Kilpatrick, I Toudjarska, et al.American Journal of Human Genetics|June 30, 2000
The ancestry of Brazilian mtDNA lineagesJ Alves-Silva, M da Silva Santos, P E Guimarães, et al.American Journal of Human Genetics|March 25, 2000
DNA pooling in mutation detection with reference to sequence analysisC I Amos, M L Frazier, W WangAmerican Journal of Human Genetics|April 11, 2000
The mutation rate in the human mtDNA control regionS Sigurğardóttir, A Helgason, J R Gulcher, et al.American Journal of Human Genetics|April 25, 2000
Unbiased application of the transmission/disequilibrium test to multilocus haplotypesF Dudbridge, B P Koeleman, J A Todd, et al.American Journal of Human Genetics|July 6, 2000
The inheritance of neuropsychological dysfunction in twins discordant for schizophreniaT D Cannon, M O Huttunen, J Lonnqvist, et al.American Journal of Human Genetics|June 10, 2000
Two genetic loci regulate T cell-dependent islet inflammation and drive autoimmune diabetes pathogenesisC J Fox, A D Paterson, S M Mortin-Toth, et al.American Journal of Human Genetics|June 10, 2000
Mapping of a new locus for autosomal recessive demyelinating Charcot-Marie-Tooth disease to 19q13.1-13.3 in a large consanguineous Lebanese family: exclusion of MAG as a candidate geneV Delague, C Bareil, S Tuffery, et al.American Journal of Human Genetics|December 5, 2002
NSD1 mutations are the major cause of Sotos syndrome and occur in some cases of Weaver syndrome but are rare in other overgrowth phenotypesJenny Douglas, Sandra Hanks, I Karen Temple, et al.Pageof 979