William S. Oetting

Linkage Analysis with Multiplexed Short Tandem Repeat Polymorphisms Using Infrared Fluorescence and M13 Tailed Primers

William S. Oetting, H. K. Lee, D. Flanders et al. · Genomics · 1995 · 374 citations

Life Sciences, Genetics, Molecular Genetics +12

Evidence That a Locus for Familial High Myopia Maps to Chromosome 18p

Terri L. Young, Shawn M. Ronan, Leslie A. Drahozal et al. · The American Journal of Human Genetics · 1998 · 309 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

A Second Locus for Familial High Myopia Maps to Chromosome 12q

Terri L. Young, Shawn M. Ronan, Alison B. Alvear et al. · The American Journal of Human Genetics · 1998 · 268 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Mutation in and lack of expression of tyrosinase-related protein-1 (TRP-1) in melanocytes from an individual with brown oculocutaneous albinism: a new subtype of albinism classified as "OCA3".

Raymond E. Boissy, Hongyi Zhao, William S. Oetting et al. · PubMed · 1996 · 195 citations · Full text

Medicine, Genetics, Molecular Genetics +8

Tyrosinase gene mutations in oculocutaneous albinism�1 (OCA1): definition of the phenotype

Richard A. King, Jacy Pietsch, James P. Fryer et al. · Human Genetics · 2003 · 170 citations

Life Sciences, Genetics, Ophthalmology +11