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Results: 1-11 |
Results: 11

Authors: WILDENBERG SC FRYER JP GARDNER JM OETTING WS BRILLIANT MH KING RA
Citation: Sc. Wildenberg et al., IDENTIFICATION OF A NOVEL TRANSCRIPT PRODUCED BY THE GENE RESPONSIBLEFOR THE HERMANSKY-PUDLAK-SYNDROME IN PUERTO-RICO, Journal of investigative dermatology, 110(5), 1998, pp. 777-781

Authors: YOUNG TL RONAN SM ALVEAR AB WILDENBERG SC OETTING WS ATWOOD LD WILKIN DJ KING RA
Citation: Tl. Young et al., A 2ND LOCUS FOR FAMILIAL HIGH MYOPIA MAPS TO CHROMOSOME 12Q, American journal of human genetics, 63(5), 1998, pp. 1419-1424

Authors: YOUNG TL RONAN SM DRAHOZAL LA WILDENBERG SC ALVEAR AB OETTING WS ATWOOD LD WILKIN DJ KING RA
Citation: Tl. Young et al., EVIDENCE THAT A LOCUS FOR FAMILIAL HIGH MYOPIA MAPS TO CHROMOSOME 18P, American journal of human genetics, 63(1), 1998, pp. 109-119

Authors: GARDNER JM WILDENBERG SC KEIPER NM NOVAK EK RUSINIAK ME SWANK RT PURI N FINGER JN HAGIWARA N LEHMAN AL GALES TL BAYER ME KING RA BRILLIANT MH
Citation: Jm. Gardner et al., THE MOUSE PALE EAR (EP) MUTATION IS THE HOMOLOG OF HUMAN HERMANSKY-PUDLAK-SYNDROME, Proceedings of the National Academy of Sciences of the United Statesof America, 94(17), 1997, pp. 9238-9243

Authors: HAZELWOOD S SHOTELERSUK V WILDENBERG SC CHEN D IWATA F KAISERKUPFER MI WHITE JG KING RA GAHL WA
Citation: S. Hazelwood et al., EVIDENCE FOR LOCUS HETEROGENEITY IN PUERTO-RICANS WITH HERMANSKY-PUDLAK-SYNDROME, American journal of human genetics, 61(5), 1997, pp. 1088-1094

Authors: WILDENBERG SC FRYER JP GARDNER JM OETTING WS SWANK RT BRILLIANT MH KING RA
Citation: Sc. Wildenberg et al., IDENTIFICATION OF A NOVEL CDNA ASSOCIATED WITH THE HERMANSKY-PUDLAK-SYNDROME (HPS), American journal of human genetics, 61(4), 1997, pp. 1974-1974

Authors: BOISSY RE ZHAO HQ OETTING WS AUSTIN LM WILDENBERG SC BOISSY YL ZHAO Y STURM RA HEARING VJ KING RA NORDLUND JJ
Citation: Re. Boissy et al., 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, American journal of human genetics, 58(6), 1996, pp. 1145-1156

Authors: WILDENBERG SC KING RA OETTING WS
Citation: Sc. Wildenberg et al., DETECTION OF A TSP5091 POLYMORPHISM IN THE 3' UTR OF THE HUMAN TYROSINASE-RELATED PROTEIN-1 (TYRP) GENE, Human genetics, 95(2), 1995, pp. 247-247

Authors: BOISSY RE ZHAO H OETTING WS KOBAYASHI T AUSTIN LM WILDENBERG SC BOISSY YL ZHAO Y HEARING VJ KING RA NORDLUND JJ
Citation: Re. Boissy et al., MUTATION IN AND LACK OF EXPRESSION OF TYROSINASE-RELATED PROTEIN-1 (TRP-1) IN MELANOCYTES FROM AN INDIVIDUAL WITH TYROSINASE-POSITIVE OCULOCUTANEOUS ALBINISM - A NEW SUBTYPE OF ALBINISM CLASSIFIED AS OCA3, Journal of investigative dermatology, 104(4), 1995, pp. 597-597

Authors: WILDENBERG SC OETTING WS ALMADOVAR C KRUMWIEDE M WHITE JG KING RA
Citation: Sc. Wildenberg et al., MAPPING OF A GENE FOR HERMANSKY-PUDLAK SYNDROME IN A PUERTO-RICAN POPULATION BY SCREENING POOLED DNA SAMPLES, American journal of human genetics, 57(4), 1995, pp. 127-127

Authors: WILDENBERG SC OETTING WS ALMODOVAR C KRUMWIEDE M WHITE JG KING RA
Citation: Sc. Wildenberg et al., A GENE CAUSING HERMANSKY-PUDLAK SYNDROME IN A PUERTO-RICAN POPULATIONMAPS TO CHROMOSOME 10Q2, American journal of human genetics, 57(4), 1995, pp. 755-765
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