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Human Molecular Genetics|December 2, 2005
Polymorphisms in the PON gene cluster are associated with Alzheimer diseasePorat M Erlich, Kathryn L Lunetta, L Adrienne Cupples, et al.Human Molecular Genetics|October 14, 2005
Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's diseaseKeiko Yamazaki, Dermot McGovern, Jiannis Ragoussis, et al.Human Molecular Genetics|January 1, 1994
A survey of long-range DNA polymorphisms on the human Y chromosomeM A JoblingHuman Molecular Genetics|January 1, 1994
Distribution of wild-type and common deletion forms of mtDNA in normal and respiration-deficient muscle fibers from patients with mitochondrial myopathyM Sciacco, E Bonilla, E A Schon, et al.Human Molecular Genetics|January 1, 1994
Identification of a stop mutation in five Finnish patients suffering from hereditary tyrosinemia type IM St-Louis, B Leclerc, J Laine, et al.Human Molecular Genetics|April 1, 1994
Sandwiching of a gene within 12 kb of a functional telomere and alpha satellite does not result in silencingR A Bayne, D Broccoli, M H Taggart, et al.Human Molecular Genetics|April 1, 1994
Detailed mapping of germline deletions of the von Hippel-Lindau disease tumour suppressor geneF M Richards, P A Crossey, M E Phipps, et al.Human Molecular Genetics|April 1, 1994
A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndromeH Meijer, E de Graaff, D M Merckx, et al.Human Molecular Genetics|February 1, 1994
Olfactory receptor gene cluster on human chromosome 17: possible duplication of an ancestral receptor repertoireN Ben-Arie, D Lancet, C Taylor, et al.Pageof 1,196