Showing results (51-60 of 148) with videos related to
Sort By:
Pageof 15
Genomics|March 15, 1996
Genomic organization of the human heparan sulfate-N-deacetylase/N-sulfotransferase gene: exclusion from a causative role in the pathogenesis of Treacher Collins syndromeA J Gladwin, J Dixon, S K Loftus, et al.Genomics|December 1, 1992
Mapping of the versican proteoglycan gene (CSPG2) to the long arm of human chromosome 5 (5q12-5q14)R V Iozzo, M F Naso, L A Cannizzaro, et al.Nature Genetics|December 1, 1993
Mutations in the alpha 1 subunit of the inhibitory glycine receptor cause the dominant neurologic disorder, hyperekplexiaR Shiang, S G Ryan, Y Z Zhu, et al.Genomics|December 1, 1992
Mapping of a human brain voltage-gated calcium channel to human chromosome 12p13-pterW Sun, J D McPherson, D Q Hoang, et al.American Journal of Human Genetics|August 1, 1989
Prenatal diagnosis and carrier detection of a cryptic translocation by using DNA markers from the short arm of chromosome 5J Overhauser, U Bengtsson, J McMahon, et al.Cytogenetics and Cell Genetics|January 1, 1992
Somatic cell mapping of the human cyclophilin B gene (PPIB) to chromosome 15L B Peddada, J D McPherson, R Law, et al.Genomics|September 1, 1995
Human estrogen sulfotransferase gene (STE): cloning, structure, and chromosomal localizationC Her, I A Aksoy, S Kimura, et al.Cytogenetics and Cell Genetics|January 1, 1994
Genes encoding adrenergic receptors are not clustered on the long arm of human chromosome 5S K Loftus, R Shiang, J A Warrington, et al.Genomics|November 1, 1991
Radiation hybrid map of 13 loci on the long arm of chromosome 5J A Warrington, L V Hall, L M Hinton, et al.Genomics|March 20, 1995
Cloning of the human heparan sulfate-N-deacetylase/N-sulfotransferase gene from the Treacher Collins syndrome candidate region at 5q32-q33.1J Dixon, S K Loftus, A J Gladwin, et al.Pageof 15