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Human Molecular Genetics|April 1, 1997
Identification of a self-association region within the SCA1 gene product, ataxin-1E N Burright, J D Davidson, L A Duvick, et al.Human Molecular Genetics|April 1, 1997
Tumour necrosis factor haplotypes and asthmaM F Moffatt, W O CooksonHuman Molecular Genetics|April 1, 1997
Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brainM E Ross, K M Allen, A K Srivastava, et al.Human Molecular Genetics|April 1, 1997
Identification of nine novel mutations in the hepatocyte nuclear factor 1 alpha gene associated with maturity-onset diabetes of the young (MODY3)M Vaxillaire, M Rouard, K Yamagata, et al.Human Molecular Genetics|April 1, 1997
Location of the first genetic locus, PKDr1, controlling autosomal dominant polycystic kidney disease in Han:SPRD cy/+ ratM T Bihoreau, I Ceccherini, J Browne, et al.Human Molecular Genetics|April 1, 1997
Identification of the gene encoding the human mitochondrial RNA polymerase (h-mtRPOL) by cyberscreening of the Expressed Sequence Tags databaseV Tiranti, A Savoia, F Forti, et al.Human Molecular Genetics|January 1, 1996
Applications of gene therapy to the CNSU Blömer, L Naldini, I M Verma, et al.Human Molecular Genetics|January 1, 1996
Myotonic dystrophy: will the real gene please step forward!S Harris, C Moncrieff, K JohnsonHuman Molecular Genetics|January 1, 1996
Huntington disease: new insights into the relationship between CAG expansion and diseaseJ Nasir, Y P Goldberg, M R HaydenPageof 1,196