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W S Oetting

Showing results (11-20 of 54) with videos related to

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Pigment Cell Research|October 1, 1994
Analysis of tyrosinase mutations associated with tyrosinase-related oculocutaneous albinism (OCA1)W S Oetting, R A King
Human 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 King
Biochemical and Biophysical Research Communications|September 23, 1977
Further characterization of a ribonucleotide-polymerizing enzyme from Histoplasma capsulatum. II. Possible role in cellular metabolismG Boguslawski, W S Oetting, D A Stetler
Human Molecular Genetics|July 1, 1993
A dinucleotide deletion (-delta GA115) in the tyrosinase gene responsible for type I-A (tyrosinase negative) oculocutaneous albinism in a Pakistani individualW S Oetting, J P Fryer, R A King
Metabolic, 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 King
Molecular Medicine Today|August 1, 1996
The clinical spectrum of albinism in humansW S Oetting, M H Brilliant, R A King
Molecular 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 Oetting
Human 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 Oetting
Progress in Clinical and Biological Research|January 1, 1988
Isolation of pigment genes using retroviral insertional mutagenesisW S Oetting, G L Smith, J A Brumbaugh
Human 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 King
Pageof 6

Showing results (11-20 of 54) with videos related to

Sort By:
Pageof 6
Pigment Cell Research|October 1, 1994
Analysis of tyrosinase mutations associated with tyrosinase-related oculocutaneous albinism (OCA1)W S Oetting, R A King
Human 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 King
Biochemical and Biophysical Research Communications|September 23, 1977
Further characterization of a ribonucleotide-polymerizing enzyme from Histoplasma capsulatum. II. Possible role in cellular metabolismG Boguslawski, W S Oetting, D A Stetler
Human Molecular Genetics|July 1, 1993
A dinucleotide deletion (-delta GA115) in the tyrosinase gene responsible for type I-A (tyrosinase negative) oculocutaneous albinism in a Pakistani individualW S Oetting, J P Fryer, R A King
Metabolic, 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 King
Molecular Medicine Today|August 1, 1996
The clinical spectrum of albinism in humansW S Oetting, M H Brilliant, R A King
Molecular 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 Oetting
Human 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 Oetting
Progress in Clinical and Biological Research|January 1, 1988
Isolation of pigment genes using retroviral insertional mutagenesisW S Oetting, G L Smith, J A Brumbaugh
Human 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 King
Pageof 6