Richard A. Spritz

A gene for the mouse pink-eyed dilution locus and for human type II oculocutaneous albinism

Eugene M. Rinchik, Scott J. Bultman, Bernhard Horsthemke et al. · Nature · 1993 · 415 citations

Medicine, Genetics, Molecular Genetics +14

Mutations of the P Gene in Oculocutaneous Albinism, Ocular Albinism, and Prader-Willi Syndrome Plus Albinism

Seung‐Taek Lee, Robert D. Nicholls, Sarah Bundey et al. · New England Journal of Medicine · 1994 · 233 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Hypopigmentation in the Prader-Willi syndrome correlates withP gene deletion but not with haplotype of the hemizygousP allele

Richard A. Spritz, T. U. Bailin, Robert D. Nicholls et al. · American Journal of Medical Genetics · 1997 · 95 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Mutations of the tyrosinase gene in patients with oculocutaneous albinism from various ethnic groups in Israel.

Ruth Gershoni‐Baruch, Ada Rosenmann, Sara Droetto et al. · PubMed · 1994 · 62 citations

Life Sciences, Genetics, Molecular Genetics +14

Fluorescence in Situ Hybridization Mapping of 25 Markers on Distal Human Chromosome 2q Surrounding the Human Waardenburg Syndrome, Type I (WS1) Locus (PAX3 Gene)

Jennifer M. Lu-Kuo, David C. Ward, Richard A. Spritz · Genomics · 1993 · 34 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17