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Genome Research|January 1, 1996
Transcriptional map of the Treacher Collins candidate gene regionS K Loftus, J Dixon, K Koprivnikar, et al.American Journal of Medical Genetics|April 1, 1993
Identification of a cryptic t(5;7) reciprocal translocation by fluorescent in situ hybridizationR Bernstein, M E Bocian, M J Cain, et al.American Journal of Human Genetics|February 1, 1988
Isolation of DNA markers in the direction of the Huntington disease gene from the G8 locusB Smith, D Skarecky, U Bengtsson, et al.Nucleic Acids Research|September 24, 1983
Chromosomal localization of the human c-fms oncogeneJ Groffen, N Heisterkamp, N Spurr, et al.Genomics|June 1, 1993
A physical map of 15 loci on human chromosome 5q23-q33 by two-color fluorescence in situ hybridizationD L Saltman, G M Dolganov, J A Warrington, et al.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.Pageof 14