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R A Spritz

Showing results (61-70 of 98) with videos related to

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American Journal of Human Genetics|February 1, 1991
Homozygous tyrosinase gene mutation in an American black with tyrosinase-negative (type IA) oculocutaneous albinismR A Spritz, K M Strunk, C L Hsieh, et al.
Genomics|March 20, 1995
Organization and sequence of the human P gene and identification of a new family of transport proteinsS T Lee, R D Nicholls, M T Jong, et al.
Biochemical and Biophysical Research Communications|February 17, 1998
Metal ligand-binding specificities of the tyrosinase-related proteinsM Furumura, F Solano, N Matsunaga, et al.
Clinical Genetics|December 1, 1982
Neonatal death in cousins with trisomy 10q and monosomy 4p due to a familial translocationR M Pauli, S J Kirkpatrick, L F Meisner, et al.
American Journal of Medical Genetics|July 15, 1992
Tyrosinase gene mutations in type I (tyrosinase-deficient) oculocutaneous albinism define two clusters of missense substitutionsR K Tripathi, K M Strunk, L B Giebel, et al.
The New England Journal of Medicine|February 24, 1994
Mutations of the P gene in oculocutaneous albinism, ocular albinism, and Prader-Willi syndrome plus albinismS T Lee, R D Nicholls, S Bundey, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1990
A frequent tyrosinase gene mutation in classic, tyrosinase-negative (type IA) oculocutaneous albinismL B Giebel, K M Strunk, R A King, et al.
American Journal of Human Genetics|April 1, 1994
Mutations of the tyrosinase gene in patients with oculocutaneous albinism from various ethnic groups in IsraelR Gershoni-Baruch, A Rosenmann, S Droetto, et al.
The Journal of Investigative Dermatology|January 1, 1997
Complementation of hypopigmentation in p-mutant (pink-eyed dilution) mouse melanocytes by normal human P cDNA, and defective complementation by OCA2 mutant sequencesE V Sviderskaya, D C Bennett, L Ho, et al.
Nucleic Acids Research|December 23, 1987
The human U1-70K snRNP protein: cDNA cloning, chromosomal localization, expression, alternative splicing and RNA-bindingR A Spritz, K Strunk, C S Surowy, et al.
Pageof 10

Showing results (61-70 of 98) with videos related to

Sort By:
Pageof 10
American Journal of Human Genetics|February 1, 1991
Homozygous tyrosinase gene mutation in an American black with tyrosinase-negative (type IA) oculocutaneous albinismR A Spritz, K M Strunk, C L Hsieh, et al.
Genomics|March 20, 1995
Organization and sequence of the human P gene and identification of a new family of transport proteinsS T Lee, R D Nicholls, M T Jong, et al.
Biochemical and Biophysical Research Communications|February 17, 1998
Metal ligand-binding specificities of the tyrosinase-related proteinsM Furumura, F Solano, N Matsunaga, et al.
Clinical Genetics|December 1, 1982
Neonatal death in cousins with trisomy 10q and monosomy 4p due to a familial translocationR M Pauli, S J Kirkpatrick, L F Meisner, et al.
American Journal of Medical Genetics|July 15, 1992
Tyrosinase gene mutations in type I (tyrosinase-deficient) oculocutaneous albinism define two clusters of missense substitutionsR K Tripathi, K M Strunk, L B Giebel, et al.
The New England Journal of Medicine|February 24, 1994
Mutations of the P gene in oculocutaneous albinism, ocular albinism, and Prader-Willi syndrome plus albinismS T Lee, R D Nicholls, S Bundey, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1990
A frequent tyrosinase gene mutation in classic, tyrosinase-negative (type IA) oculocutaneous albinismL B Giebel, K M Strunk, R A King, et al.
American Journal of Human Genetics|April 1, 1994
Mutations of the tyrosinase gene in patients with oculocutaneous albinism from various ethnic groups in IsraelR Gershoni-Baruch, A Rosenmann, S Droetto, et al.
The Journal of Investigative Dermatology|January 1, 1997
Complementation of hypopigmentation in p-mutant (pink-eyed dilution) mouse melanocytes by normal human P cDNA, and defective complementation by OCA2 mutant sequencesE V Sviderskaya, D C Bennett, L Ho, et al.
Nucleic Acids Research|December 23, 1987
The human U1-70K snRNP protein: cDNA cloning, chromosomal localization, expression, alternative splicing and RNA-bindingR A Spritz, K Strunk, C S Surowy, et al.
Pageof 10