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Human Genetics|January 15, 2008
Congenital, low penetrance lymphedema of lower limbs maps to chromosome 6q16.2-q22.1 in an inbred Pakistani familySajid Malik, Karl-Heinz GrzeschikHuman Genetics|January 29, 2008
A new locus for otosclerosis, OTSC8, maps to the pericentromeric region of chromosome 9Insaf Bel Hadj Ali, Melissa Thys, Najeh Beltaief, et al.Human Genetics|January 23, 2008
Exploring gene-environment interactions in Parkinson's diseaseColin C McCulloch, Denise M Kay, Stewart A Factor, et al.Human Genetics|March 7, 2008
Pax6 3' deletion results in aniridia, autism and mental retardationL K Davis, K J Meyer, D S Rudd, et al.Human Genetics|March 6, 2008
Maternal cigarette smoking, metabolic gene polymorphisms, and preterm delivery: new insights on GxE interactions and pathogenic pathwaysHui-Ju Tsai, Xin Liu, Karen Mestan, et al.Human Genetics|March 20, 2008
A haplotype at chromosome Xq27.2 confers susceptibility to prostate cancerBrian L Yaspan, Kate M McReynolds, J Bradford Elmore, et al.Human Genetics|March 29, 2008
Common polymorphisms of ALOX5 and ALOX5AP and risk of coronary artery diseaseThemistocles L Assimes, Joshua W Knowles, James R Priest, et al.Human Genetics|September 1, 1991
Synthesis of glycosaminoglycans in fibroblasts from abortuses with trisomy, triploidy, and from children with Down's syndromeV I Kukharenko, E M Pichugina, M I Freidin, et al.Human Genetics|June 30, 1977
Nonlinkage between C6 and chromosome 6 markersJ H Olving, B Olaisen, P Teisberg, et al.Human Genetics|June 30, 1977
Full monosomy 21: a clinically recognizable syndrome?J P Fryns, F D'Hondt, P Goddeeris, et al.Pageof 957