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Annals of the New York Academy of Sciences|January 1, 1991
Genetic heterogeneity in tuberous sclerosis. Study of a large collaborative datasetJ L Haines, J Amos, J Attwood, et al.
The Pharmacogenomics Journal|February 28, 2008
Genome-wide approaches to identify pharmacogenetic contributions to adverse drug reactionsM R Nelson, S-A Bacanu, M Mosteller, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|December 1, 1993
Localization of Shaw-related K+ channel genes on mouse and human chromosomesM Haas, D C Ward, J Lee, et al.
American Journal of Medical Genetics|October 1, 1987
Chorea-acanthocytosis: a report of three new families and implications for genetic counsellingJ M Vance, M A Pericak-Vance, M H Bowman, et al.
Cytogenetics and Cell Genetics|January 1, 1996
Complete coding sequence, exon/intron arrangement and chromosome location of ZNF45, a KRAB-domain-containing geneC Constantinou Deltas, E Bashiardes, P C Patsalis, et al.
Somatic Cell and Molecular Genetics|January 1, 1993
A genetic linkage map of the chromosome 4 short armP A Locke, M E MacDonald, J Srinidhi, et al.
Genomics|September 1, 1990
Autosomal dominant retinitis pigmentosa: linkage to rhodopsin and evidence for genetic heterogeneityG J Farrar, P McWilliam, D G Bradley, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 30, 1994
Relative abundance of Alzheimer A beta amyloid peptide variants in Alzheimer disease and normal agingJ Näslund, A Schierhorn, U Hellman, et al.
Muscle & Nerve|June 1, 1983
Recombinant DNA strategies in genetic neurological diseasesA D Roses, M A Pericak-Vance, L H Yamaoka, et al.
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