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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.Genomics|March 1, 1992
Localization of the D5 dopamine receptor gene to human chromosome 4p15.1-p15.3, centromeric to the Huntington's disease locusJ H Eubanks, M Altherr, C Wagner-McPherson, et al.Cytogenetics and Cell Genetics|January 1, 1993
Linkage mapping detects two secondary microdeletions in cell hybrid HHW1064, used to isolate DNA probes from within 5q11.2-->q13.3L E Bernard, J D McPherson, J J Wasmuth, et al.Genomics|April 1, 1992
Chromosome mapping of the rod photoreceptor cGMP phosphodiesterase beta-subunit gene in mouse and human: tight linkage to the Huntington disease region (4p16.3)M R Altherr, J J Wasmuth, M F Seldin, et al.American Journal of Medical Genetics|September 1, 1990
Parental origin of chromosome 5 deletions in the cri-du-chat syndromeJ Overhauser, J McMahon, S Oberlender, et al.Human Molecular Genetics|November 1, 1993
A combined genetic and radiation hybrid map surrounding the Treacher Collins syndrome locus on chromosome 5qS K Loftus, S J Edwards, T Scherpbier-Heddema, et al.Pageof 14