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Human Molecular Genetics|November 2, 2001
Functional variation of MC1R alleles from red-haired individualsE Healy, S A Jordan, P S Budd, et al.Genome Research|February 1, 1997
Mapping in the region of Danforth's short tail and the localization of tail length modifiersJ B Alfred, K Rance, B A Taylor, et al.Genetics|July 1, 1994
Molecular genetics of the brown (b)-locus region of mouse chromosome 4. I. Origin and molecular mapping of radiation- and chemical-induced lethal brown deletionsE M Rinchik, J A Bell, P R Hunsicker, et al.Annals of the New York Academy of Sciences|January 1, 1991
Reverse genetics in the mouse and its application to the study of deafnessE M Rinchik, D K Johnson, F L Margolis, et al.The EMBO Journal|February 1, 1992
A second tyrosinase-related protein, TRP-2, maps to and is mutated at the mouse slaty locusI J Jackson, D M Chambers, K Tsukamoto, et al.Nucleic Acids Research|January 24, 1981
The absence of introns within a human fibroblast interferon geneM Houghton, I J Jackson, A G Porter, et al.Human Molecular Genetics|October 1, 1996
The Asp84Glu variant of the melanocortin 1 receptor (MC1R) is associated with melanomaP Valverde, E Healy, S Sikkink, et al.Genomics|August 1, 1994
Genetic and physical mapping of a gene encoding a methyl CpG binding protein, Mecp2, to the mouse X chromosomeN A Quaderi, R R Meehan, P H Tate, et al.Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 3, 2000
CpG island libraries from human chromosomes 18 and 22: landmarks for novel genesS H Cross, V H Clark, M W Simmen, et al.Human Molecular Genetics|October 13, 2000
Pleiotropic effects of the melanocortin 1 receptor (MC1R) gene on human pigmentationN Flanagan, E Healy, A Ray, et al.Pageof 10