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Human Genetics|November 1, 1992
Molecular analysis of type I-A (tyrosinase negative) oculocutaneous albinismW S Oetting, R A KingPigment Cell Research|January 1, 1992
Molecular basis of type IA (tyrosinase negative) oculocutaneous albinismR A King, W S OettingThe Journal of Investigative Dermatology|November 1, 1994
Molecular basis of oculocutaneous albinismW S Oetting, R A KingPigment Cell Research|October 1, 1994
Analysis of tyrosinase mutations associated with tyrosinase-related oculocutaneous albinism (OCA1)W S Oetting, R A KingHuman Mutation|January 1, 1993
Molecular basis of type I (tyrosinase-related) oculocutaneous albinism: mutations and polymorphisms of the human tyrosinase geneW S Oetting, R A KingMetabolic, Pediatric, and Systemic Ophthalmology (New York, N.Y. : 1985)|January 1, 1994
Albinism and the associated ocular defectsW S Oetting, C G Summers, R A KingMolecular Medicine Today|August 1, 1996
The clinical spectrum of albinism in humansW S Oetting, M H Brilliant, R A KingMolecular Biology & Medicine|February 1, 1991
Non-random distribution of missense mutations within the human tyrosinase gene in type I (tyrosinase-related) oculocutaneous albinismR A King, M M Mentink, W S OettingHuman Genetics|February 1, 1995
Detection of a Tsp509I polymorphism in the 3' UTR of the human tyrosinase related protein-1 (TYRP) geneS C Wildenberg, R A King, W S OettingHuman Mutation|February 12, 2000
Mutations of the human tyrosinase gene associated with tyrosinase related oculocutaneous albinism (OCA1). Mutations in brief no. 204. OnlineW S Oetting, J P Fryer, R A KingPageof 36