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American Journal of Human Genetics|February 15, 2001
Problems in the definition, interpretation, and evaluation of genetic heterogeneityA S Whittemore, J HalpernAmerican Journal of Human Genetics|June 19, 2001
High-resolution multipoint linkage-disequilibrium mapping in the context of a human genome sequenceB Rannala, J P ReeveAmerican Journal of Human Genetics|June 9, 2001
Linkage of otopalatodigital syndrome type 2 (OPD2) to distal Xq28: evidence for allelism with OPD1S P Robertson, S Walsh, M Oldridge, et al.American Journal of Human Genetics|June 9, 2001
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1FZ M Ahmed, S Riazuddin, S L Bernstein, et al.American Journal of Human Genetics|June 19, 2001
Are rare variants responsible for susceptibility to complex diseases?J K PritchardAmerican Journal of Human Genetics|June 19, 2001
Multifactor-dimensionality reduction reveals high-order interactions among estrogen-metabolism genes in sporadic breast cancerM D Ritchie, L W Hahn, N Roodi, et al.American Journal of Human Genetics|June 13, 2001
A common ancestral origin of the frequent and widespread 2299delG USH2A mutationB Dreyer, L Tranebjaerg, V Brox, et al.American Journal of Human Genetics|April 28, 2001
Benign familial infantile convulsions: mapping of a novel locus on chromosome 2q24 and evidence for genetic heterogeneityM Malacarne, E Gennaro, F Madia, et al.American Journal of Human Genetics|May 12, 2001
Niemann-Pick C variant detection by altered sphingolipid trafficking and correlation with mutations within a specific domain of NPC1X Sun, D L Marks, W D Park, et al.American Journal of Human Genetics|May 12, 2001
Large-scale deletion and point mutations of the nuclear NDUFV1 and NDUFS1 genes in mitochondrial complex I deficiencyP Bénit, D Chretien, N Kadhom, et al.Pageof 980