A Second Locus for Familial High Myopia Maps to Chromosome 12q
Young, Terri L., Ronan, Shawn M., Alvear, Alison B., Wildenberg, Scott C., Oetting, William S., Atwood, Larry D., Wilkin, Douglas J., King, Richard A.
Published in American journal of human genetics (01.11.1998)
Published in American journal of human genetics (01.11.1998)
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Journal Article
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
BOISSY, R. E, ZHAO, H, NORDLUND, J. J, OETTING, W. S, AUSTIN, L. M, WILDENBERG, S. C, BOISSY, Y. L, ZHAO, Y, STURM, R. A, HEARING, V. J, KING, R. A
Published in American journal of human genetics (01.06.1996)
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Published in American journal of human genetics (01.06.1996)
Journal Article
Evidence That a Locus for Familial High Myopia Maps to Chromosome 18p
Young, Terri L., Ronan, Shawn M., Drahozal, Leslie A., Wildenberg, Scott C., Alvear, Alison B., Oetting, William S., Atwood, Larry D., Wilkin, Douglas J., King, Richard A.
Published in American journal of human genetics (01.07.1998)
Published in American journal of human genetics (01.07.1998)
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Journal Article
A gene causing Hermansky-Pudlak syndrome in a Puerto Rican population maps to chromosome 10q2
WILDENBERG, S. C, OETTING, W. S, ALMODOVAR, C, KRUMWIEDE, M, WHITE, J. G, KING, R. A
Published in American journal of human genetics (01.10.1995)
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Published in American journal of human genetics (01.10.1995)
Journal Article
Evidence for Locus Heterogeneity in Puerto Ricans with Hermansky-Pudlak Syndrome
Hazelwood, Senator, Shotelersuk, Vorasuk, Wildenberg, Scott C., Chen, David, Iwata, Fumino, Kaiser-Kupfer, Muriel I., White, James G., King, Richard A., Gahl, William A.
Published in American journal of human genetics (01.11.1997)
Published in American journal of human genetics (01.11.1997)
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Journal Article
Identification of a Novel Transcript Produced by the Gene Responsible for the Hermansky–Pudlak Syndrome in Puerto Rico
Wildenberg, Scott C., Fryer, James P., Gardner, John M., Brilliant, Murray H., Oetting, William S., King, Richard A.
Published in Journal of investigative dermatology (01.05.1998)
Published in Journal of investigative dermatology (01.05.1998)
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Journal Article
The Mouse Pale Ear (ep) Mutation is the Homologue of Human Hermansky-Pudlak Syndrome
Gardner, John M., Wildenberg, Scott C., Keiper, Natalie M., Novak, Edward K., Rusiniak, Michael E., Swank, Richard T., Puri, Neelu, Finger, Joshua N., Hagiwara, Nobuko, Lehman, Anne L., Gales, Tracy L., Bayer, Manfred E., King, Richard A., Brilliant, Murray H.
Published in Proceedings of the National Academy of Sciences - PNAS (19.08.1997)
Published in Proceedings of the National Academy of Sciences - PNAS (19.08.1997)
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Journal Article
New Locus for Autosomal Dominant High Myopia Maps to the Long Arm of Chromosome 17
Paluru, Prasuna, Ronan, Shawn M, Heon, Elise, Devoto, Marcella, Wildenberg, Scott C, Scavello, Genaro, Holleschau, Ann, Makitie, Outi, Cole, William G, King, Richard A, Young, Terri L
Published in Investigative ophthalmology & visual science (01.05.2003)
Published in Investigative ophthalmology & visual science (01.05.2003)
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Journal Article
Mutation in and lack of expression of tyrosine-related protein-1 (TRP-1) in melanocytes from an individual with brown oculocutaneous albinism: A new subtype of albinism classified as "OCA3"
Boissy, R E, Zhao, H, Oetting, W S, Austin, L M, Wildenberg, S C, Boissy, Y L, Zhao, Y, Sturm, R A, Hearing, V J
Published in American journal of human genetics (01.01.1996)
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Published in American journal of human genetics (01.01.1996)
Journal Article