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Genomics|October 10, 1995
Cloning and characterization of CLCN5, the human kidney chloride channel gene implicated in Dent disease (an X-linked hereditary nephrolithiasis)S E Fisher, I van Bakel, S E Lloyd, et al.Genomics|October 1, 1991
A deletion map of the human Yq11 region: implications for the evolution of the Y chromosome and tentative mapping of a locus involved in spermatogenesisB Bardoni, O Zuffardi, S Guioli, et al.Journal of Medical Genetics|April 1, 1987
Localisation of Y chromosome sequences in normal and 'XX' malesV J Buckle, Y Boyd, N Fraser, et al.American Journal of Medical Genetics|February 2, 1996
Autosomal dominant transmission of familial laterality defectsB Casey, B F Cuneo, C Vitali, et al.Nature Genetics|November 4, 2000
The nicotinic receptor beta 2 subunit is mutant in nocturnal frontal lobe epilepsyM De Fusco, A Becchetti, A Patrignani, et al.Human Molecular Genetics|July 1, 1994
A YAC-based binning strategy facilitating the rapid assembly of cosmid contigs: 1.6 Mb of overlapping cosmids in Xp22M C Wapenaar, M V Schiaffino, M T Bassi, et al.Mechanisms of Development|September 3, 1999
Expression pattern of the Tbr2 (Eomesodermin) gene during mouse and chick brain developmentA Bulfone, S Martinez, V Marigo, et al.Molecular Psychiatry|July 9, 2004
Gene-environment interaction analysis of serotonin system markers with adolescent depressionT C Eley, K Sugden, A Corsico, et al.Human Molecular Genetics|November 1, 1994
Isolation and partial characterization of a chloride channel gene which is expressed in kidney and is a candidate for Dent's disease (an X-linked hereditary nephrolithiasis)S E Fisher, G C Black, S E Lloyd, et al.Eye (London, England)|January 1, 1995
Leber's hereditary optic neuropathy: implications of the sex ratio for linkage studies in families with the 3460 ND1 mutationG C Black, I W Craig, R J Oostra, et al.Pageof 30