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American Journal of Human Genetics|May 2, 2000
Genomic differentiation of Neanderthals and anatomically modern man allows a fossil-DNA-based classification of morphologically indistinguishable hominid bonesM Scholz, L Bachmann, G J Nicholson, et al.American Journal of Human Genetics|April 25, 2000
Genomewide search in Canadian families with inflammatory bowel disease reveals two novel susceptibility lociJ D Rioux, M S Silverberg, M J Daly, et al.American Journal of Human Genetics|April 25, 2000
Gaucher disease: the origins of the Ashkenazi Jewish N370S and 84GG acid beta-glucosidase mutationsG A Diaz, B D Gelb, N Risch, et al.American Journal of Human Genetics|May 4, 2000
Genomewide search for type 2 diabetes susceptibility genes in four American populationsM G Ehm, M C Karnoub, H Sakul, et al.American Journal of Human Genetics|December 1, 1999
Phenotypes in three pedigrees with autosomal dominant obesity caused by haploinsufficiency mutations in the melanocortin-4 receptor geneM Sina, A Hinney, A Ziegler, et al.American Journal of Human Genetics|December 1, 1999
Loss-of-function mutations in a human gene related to Chlamydomonas reinhardtii dynein IC78 result in primary ciliary dyskinesiaG Pennarun, E Escudier, C Chapelin, et al.American Journal of Human Genetics|December 1, 1999
Rett syndrome and beyond: recurrent spontaneous and familial MECP2 mutations at CpG hotspotsM Wan, S S Lee, X Zhang, et al.American Journal of Human Genetics|December 1, 1999
The molecular basis of Sjögren-Larsson syndrome: mutation analysis of the fatty aldehyde dehydrogenase geneW B Rizzo, G Carney, Z LinAmerican Journal of Human Genetics|December 1, 1999
A common breakpoint on 11q23 in carriers of the constitutional t(11;22) translocationL Edelmann, E Spiteri, N McCain, et al.American Journal of Human Genetics|December 1, 1999
Accelerated telomere shortening in the human inactive X chromosomeJ Surrallés, M P Hande, R Marcos, et al.Pageof 979