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FEBS Letters|June 28, 1993
X-linked Kallmann syndrome. A neuronal targeting defect in the olfactory system?B Lutz, E I Rugarli, G Eichele, et al.Trends in Biotechnology|January 13, 2000
Chasing behaviour genes into the next millenniumI W Craig, J McClay, R Plomin, et al.Journal of Neurochemistry|November 1, 1982
Immunological studies of human monoamine oxidasesG K Brown, J F Powell, I W CraigGenomics|November 1, 1988
Mapping of Xp21 translocation breakpoints in and around the DMD gene by pulsed field gel electrophoresisT Meitinger, Y Boyd, R Anand, et al.Annals of Human Genetics|May 1, 1989
Assignment of the coding sequence for carcinoembryonic antigen (CEA) and normal cross-reacting antigen (NCA) to human chromosome 19q13T C Willcocks, S P Craig, I W CraigAmerican Journal of Human Genetics|March 1, 1992
Identification of point mutations in the steroid sulfatase gene of three patients with X-linked ichthyosisE Basler, M Grompe, G Parenti, et al.Development (Cambridge, England)|January 1, 1987
Identification of incomplete coding sequences for steroid sulphatase on the human Y chromosome: evidence for an ancestral pseudoautosomal gene?N Fraser, A Ballabio, M Zollo, et al.Genomics|October 1, 1990
Two families of low-copy-number repeats are interspersed on Xp22.3: implications for the high frequency of deletions in this regionA Ballabio, B Bardoni, S Guioli, et al.Human Molecular Genetics|March 7, 2001
WBSCR14, a gene mapping to the Williams--Beuren syndrome deleted region, is a new member of the Mlx transcription factor networkS Cairo, G Merla, F Urbinati, et al.Bioinformatics (Oxford, England)|March 25, 1999
TargetFinder: searching annotated sequence databases for target genes of transcription factorsG Lavorgna, A Guffanti, G Borsani, et al.Pageof 30