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
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