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R A Spritz

Showing results (81-90 of 98) with videos related to

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American Journal of Human Genetics|December 1, 1993
Mutations of the tyrosinase gene in Indo-Pakistani patients with type I (tyrosinase-deficient) oculocutaneous albinism (OCA)R K Tripathi, S Bundey, M A Musarella, et al.
American Journal of Human Genetics|September 1, 1996
Homozygosity mapping of the gene for Chediak-Higashi syndrome to chromosome 1q42-q44 in a segment of conserved synteny that includes the mouse beige locus (bg)K Fukai, J Oh, M A Karim, et al.
American Journal of Medical Genetics|July 11, 1997
Hypopigmentation in the Prader-Willi syndrome correlates with P gene deletion but not with haplotype of the hemizygous P alleleR A Spritz, T Bailin, R D Nicholls, et al.
Nature Genetics|January 1, 1995
Autosomal recessive ocular albinism associated with a functionally significant tyrosinase gene polymorphismK Fukai, S A Holmes, N J Lucchese, et al.
Journal of Evolutionary Biology|May 29, 2016
Genetic structure of phenotypic robustness in the collaborative cross mouse diallel panelP N Gonzalez, M Pavlicev, P Mitteroecker, et al.
Nature Genetics|November 1, 1996
Positional cloning of a gene for Hermansky-Pudlak syndrome, a disorder of cytoplasmic organellesJ Oh, T Bailin, K Fukai, et al.
American Journal of Human Genetics|June 1, 1991
Tyrosinase gene mutations associated with type IB ("yellow") oculocutaneous albinismL B Giebel, R K Tripathi, K M Strunk, et al.
Gene|December 8, 1993
The human TYRO3 gene and pseudogene are located in chromosome 15q14-q25A Polvi, E Armstrong, C Lai, et al.
Human Molecular Genetics|November 1, 1994
Diverse mutations of the P gene among African-Americans with type II (tyrosinase-positive) oculocutaneous albinism (OCA2)S T Lee, R D Nicholls, R E Schnur, et al.
Nature|January 7, 1993
A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinismE M Rinchik, S J Bultman, B Horsthemke, et al.
Pageof 10

Showing results (81-90 of 98) with videos related to

Sort By:
Pageof 10
American Journal of Human Genetics|December 1, 1993
Mutations of the tyrosinase gene in Indo-Pakistani patients with type I (tyrosinase-deficient) oculocutaneous albinism (OCA)R K Tripathi, S Bundey, M A Musarella, et al.
American Journal of Human Genetics|September 1, 1996
Homozygosity mapping of the gene for Chediak-Higashi syndrome to chromosome 1q42-q44 in a segment of conserved synteny that includes the mouse beige locus (bg)K Fukai, J Oh, M A Karim, et al.
American Journal of Medical Genetics|July 11, 1997
Hypopigmentation in the Prader-Willi syndrome correlates with P gene deletion but not with haplotype of the hemizygous P alleleR A Spritz, T Bailin, R D Nicholls, et al.
Nature Genetics|January 1, 1995
Autosomal recessive ocular albinism associated with a functionally significant tyrosinase gene polymorphismK Fukai, S A Holmes, N J Lucchese, et al.
Journal of Evolutionary Biology|May 29, 2016
Genetic structure of phenotypic robustness in the collaborative cross mouse diallel panelP N Gonzalez, M Pavlicev, P Mitteroecker, et al.
Nature Genetics|November 1, 1996
Positional cloning of a gene for Hermansky-Pudlak syndrome, a disorder of cytoplasmic organellesJ Oh, T Bailin, K Fukai, et al.
American Journal of Human Genetics|June 1, 1991
Tyrosinase gene mutations associated with type IB ("yellow") oculocutaneous albinismL B Giebel, R K Tripathi, K M Strunk, et al.
Gene|December 8, 1993
The human TYRO3 gene and pseudogene are located in chromosome 15q14-q25A Polvi, E Armstrong, C Lai, et al.
Human Molecular Genetics|November 1, 1994
Diverse mutations of the P gene among African-Americans with type II (tyrosinase-positive) oculocutaneous albinism (OCA2)S T Lee, R D Nicholls, R E Schnur, et al.
Nature|January 7, 1993
A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinismE M Rinchik, S J Bultman, B Horsthemke, et al.
Pageof 10