Showing results (3001-3010 of 9,807) with videos related to

Sort By:
Pageof 981
American Journal of Human Genetics|May 29, 2000
Additional copies of the proteolipid protein gene causing Pelizaeus-Merzbacher disease arise by separate integration into the X chromosomeM E Hodes, K Woodward, N B Spinner, et al.
American Journal of Human Genetics|May 29, 2000
The exon 13 duplication in the BRCA1 gene is a founder mutation present in geographically diverse populations. The BRCA1 Exon 13 Duplication Screening Group
American Journal of Human Genetics|June 3, 2000
Bayesian fine-scale mapping of disease loci, by hidden Markov modelsA P Morris, J C Whittaker, D J Balding
American Journal of Human Genetics|April 14, 2000
Power of linkage versus association analysis of quantitative traits, by use of variance-components models, for sibship dataP C Sham, S S Cherny, S Purcell, et al.
American Journal of Human Genetics|April 14, 2000
Detection of the signature of natural selection in humans: evidence from the Duffy blood group locusM T Hamblin, A Di Rienzo
American Journal of Human Genetics|April 25, 2000
Identification of uniparental disomy following prenatal detection of Robertsonian translocations and isochromosomesS A Berend, J Horwitz, C McCaskill, et al.
American Journal of Human Genetics|April 25, 2000
Intragenic inversion of mtDNA: a new type of pathogenic mutation in a patient with mitochondrial myopathyO Musumeci, A L Andreu, S Shanske, et al.
American Journal of Human Genetics|May 29, 2000
Genomewide scan for prostate cancer-aggressiveness lociJ S Witte, K A Goddard, D V Conti, et al.
American Journal of Human Genetics|March 11, 2000
High germinal instability of the (CTG)n at the SCA8 locus of both expanded and normal allelesI Silveira, I Alonso, L Guimarães, et al.
American Journal of Human Genetics|March 11, 2000
Two new loci for autosomal recessive ichthyosis on chromosomes 3p21 and 19p12-q12 and evidence for further genetic heterogeneityJ Fischer, A Faure, B Bouadjar, et al.
Pageof 981