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Human Molecular Genetics|November 13, 1998
Localization of myotonic dystrophy protein kinase in human and rabbit tissues using a new panel of monoclonal antibodiesY C Pham, N Man, L T Lam, et al.Human Molecular Genetics|May 1, 1997
Apparent digenic inheritance of Waardenburg syndrome type 2 (WS2) and autosomal recessive ocular albinism (AROA)R Morell, R A Spritz, L Ho, et al.Human Molecular Genetics|May 1, 1997
Autosomal dominant cerulean cataract is associated with a chain termination mutation in the human beta-crystallin gene CRYBB2M Litt, R Carrero-Valenzuela, D M LaMorticella, et al.Human Molecular Genetics|May 1, 1997
Homozygosity mapping of achromatopsia to chromosome 2 using DNA poolingN C Arbour, J Zlotogora, R G Knowlton, et al.Human Molecular Genetics|May 1, 1997
Reduced penetrance of the Huntington's disease mutationS M McNeil, A Novelletto, J Srinidhi, et al.Human Molecular Genetics|May 1, 1997
Identification of a major susceptibility locus on chromosome 6p and evidence for further disease loci revealed by a two stage genome-wide search in psoriasisR C Trembath, R L Clough, J L Rosbotham, et al.Human Molecular Genetics|January 26, 2006
DNA copy-number analysis in bipolar disorder and schizophrenia reveals aberrations in genes involved in glutamate signalingGary M Wilson, Stephane Flibotte, Vikramjit Chopra, et al.Human Molecular Genetics|January 26, 2006
Podocalyxin variants and risk of prostate cancer and tumor aggressivenessGraham Casey, Phillippa J Neville, Xin Liu, et al.Human Molecular Genetics|February 16, 2006
Absence of alpha 7 integrin in dystrophin-deficient mice causes a myopathy similar to Duchenne muscular dystrophyChun Guo, Michael Willem, Alexander Werner, et al.Human Molecular Genetics|January 18, 2006
Mild Nijmegen breakage syndrome phenotype due to alternative splicingRaymonda Varon, Véronique Dutrannoy, Georg Weikert, et al.Pageof 1,196