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발행년	- (예 : 2010-2015)

New locus for autosomal dominant high myopia maps to the long arm of chromosome 17

Academic Journal

Paluru, P.; Scavello, G.; Young, T.L.; Ronan, S.M.; Wildenberg, S.C.; Holleschau, A.; Heon, E.; Devoto, M.; Mäkitie, O.; Cole, W.G.; King, R.A.

In: Investigative Ophthalmology and Visual Science. (Investigative Ophthalmology and Visual Science, 1 May 2003, 44(5):1830-1836)

Open Access (EBSCO) Web of Science JCR 저널정보 Scopus Find it@PNU

Identification of a novel transcript produced by the gene responsible for the Hermansky-Pudlak syndrome in Puerto Rico

Academic Journal

Wildenberg, S.C.; Fryer, J.P.; Oetting, W.S.; King, R.A.; Gardner, J.M.; Brilliant, M.H.

In: Journal of Investigative Dermatology. (Journal of Investigative Dermatology, 1998, 110(5):777-781)

Full Text (ScienceDirect 종량제) Full Text (ScienceDirect O/A) Open Access (EBSCO) Web of Science JCR 저널정보 Scopus Find it@PNU

Evidence that a locus for familial high myopia maps to chromosome 18p

Academic Journal

Young, T.L.; Ronan, S.M.; Drahozal, L.A.; Alvear, A.B.; Wildenberg, S.C.; Oetting, W.S.; King, R.A.; Atwood, L.D.; Wilkin, D.J.

In: American Journal of Human Genetics. (American Journal of Human Genetics, July 1998, 63(1):109-119)

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A second locus for familial high myopia maps to chromosome 12q

Academic Journal

Young, T.L.; Ronan, S.M.; Alvear, A.B.; Wildenberg, S.C.; Oetting, W.S.; King, R.A.; Atwood, L.D.; Wilkin, D.J.

In: American Journal of Human Genetics. (American Journal of Human Genetics, 1998, 63(5):1419-1424)

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The mouse pale ear (ep) mutation is the homologue of human Hermansky-Pudlak syndrome

Academic Journal

Gardner, J.M.; Keiper, N.M.; Puri, N.; Finger, J.N.; Hagiwara, N.; Lehman, A.L.; Gales, T.L.; Bayer, M.E.; Brilliant, M.H.; Wildenberg, S.C.; King, R.A.; Novak, E.K.; Rusiniak, M.E.; Swank, R.T.

In: Proceedings of the National Academy of Sciences of the United States of America. (Proceedings of the National Academy of Sciences of the United States of America, 19 August 1997, 94(17):9238-9243)

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Evidence for locus heterogeneity in Puerto Ricans with Hermansky-Pudlak syndrome

Academic Journal

Hazelwood, S.; Shotelersuk, V.; Chen, D.; Gahl, W.A.; Kaiser-Kupfer, M.I.; Wildenberg, S.C.; Iwata, F.; King, R.A.; White, J.G.

In: American Journal of Human Genetics. (American Journal of Human Genetics, November 1997, 61(5):1088-1094)

Open Access (EBSCO) Web of Science JCR 저널정보 Scopus Find it@PNU

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'

Academic Journal

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.; King, R.A.; Nordlund, J.J.

In: American Journal of Human Genetics. (American Journal of Human Genetics, 1996, 58(6):1145-1156)

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Detection of a Tsp509I polymorphism in the 3′ UTR of the human tyrosinase related protein-1 (TYRP) gene

Academic Journal

Wildenberg, S.C.; King, R.A.; Oetting, W.S.

In: Human Genetics. (Human Genetics, February 1995, 95(2):247)

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A gene causing Hermansky-Pudlak syndrome in a Puerto Rican population maps to chromosome 10q2

Academic Journal

Wildenberg, S.C.; Oetting, W.S.; King, R.A.; Krumwiede, M.; White, J.G.; Almodóvar, C.

In: American Journal of Human Genetics. (American Journal of Human Genetics, 1995, 57(4):755-765)

Web of Science JCR 저널정보 Scopus Find it@PNU

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