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Results: 1-23 |
Results: 23
IDENTIFICATION OF A NOVEL TRANSCRIPT PRODUCED BY THE GENE RESPONSIBLEFOR THE HERMANSKY-PUDLAK-SYNDROME IN PUERTO-RICO
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
A 2ND LOCUS FOR FAMILIAL HIGH MYOPIA MAPS TO CHROMOSOME 12Q
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
EVIDENCE THAT A LOCUS FOR FAMILIAL HIGH MYOPIA MAPS TO CHROMOSOME 18P
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
LINKAGE ANALYSIS OF FAMILIAL PATHOLOGICAL MYOPIA
Authors: YOUNG TL RONAN SM OETTING WS ATWOOD LD KING RA
Citation: Tl. Young et al., LINKAGE ANALYSIS OF FAMILIAL PATHOLOGICAL MYOPIA, Investigative ophthalmology & visual science, 38(4), 1997, pp. 1360-1360
MULTIPLEXED SHORT TANDEM REPEAT POLYMORPHISMS OF THE WEBER 8A SET OF MARKERS USING DUAL DYE INFRARED FLUORESCENCE AND M13 TAILED PRIMERS
Authors: OETTING WS ARMSTRONGJACOBS CM RONAN SM YOUNG TL SELLERS TA KING RA
Citation: Ws. Oetting et al., MULTIPLEXED SHORT TANDEM REPEAT POLYMORPHISMS OF THE WEBER 8A SET OF MARKERS USING DUAL DYE INFRARED FLUORESCENCE AND M13 TAILED PRIMERS, American journal of human genetics, 61(4), 1997, pp. 1684-1684
IDENTIFICATION OF A NOVEL CDNA ASSOCIATED WITH THE HERMANSKY-PUDLAK-SYNDROME (HPS)
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
THE CLINICAL SPECTRUM OF ALBINISM IN HUMANS
Authors: OETTING WS BRILLIANT MH KING RA
Citation: Ws. Oetting et al., THE CLINICAL SPECTRUM OF ALBINISM IN HUMANS, Molecular medicine today, 2(8), 1996, pp. 330-335
ANALYSIS OF MULTIPLEX FAMILIES CONTAINING ASTHMA USING POOLED DNA ANALYSIS
Authors: BROTT MJ FLANDERS DJ OETTING WS KING RA BLUMENTHAL MN
Citation: Mj. Brott et al., ANALYSIS OF MULTIPLEX FAMILIES CONTAINING ASTHMA USING POOLED DNA ANALYSIS, Journal of allergy and clinical immunology, 97(1), 1996, pp. 936-936
DIAGNOSIS OF OCULOCUTANEOUS ALBINISM WITH MOLECULAR ANALYSIS
Authors: SUMMERS CG OETTING WS KING RA
Citation: Cg. Summers et al., DIAGNOSIS OF OCULOCUTANEOUS ALBINISM WITH MOLECULAR ANALYSIS, American journal of ophthalmology, 121(6), 1996, pp. 724-726
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
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
LINKAGE ANALYSIS WITH MULTIPLEXED SHORT TANDEM REPEAT POLYMORPHISMS USING INFRARED FLUORESCENCE AND M13 TAILED PRIMERS
Authors: OETTING WS LEE HK FLANDERS DJ WIESNER GL SELLERS TA KING RA
Citation: Ws. Oetting et al., LINKAGE ANALYSIS WITH MULTIPLEXED SHORT TANDEM REPEAT POLYMORPHISMS USING INFRARED FLUORESCENCE AND M13 TAILED PRIMERS, Genomics, 30(3), 1995, pp. 450-458
DETECTION OF A TSP5091 POLYMORPHISM IN THE 3' UTR OF THE HUMAN TYROSINASE-RELATED PROTEIN-1 (TYRP) GENE
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
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
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
MAPPING OF A GENE FOR HERMANSKY-PUDLAK SYNDROME IN A PUERTO-RICAN POPULATION BY SCREENING POOLED DNA SAMPLES
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
MUTATIONS AND POLYMORPHISMS OF THE HUMAN P-GENE ASSOCIATED WITH P-RELATED OCULOCUTANEOUS ALBINISM (OCA2)
Authors: OETTING WS BRILLIANT MH GARDINER JM FRYER JP KING RA
Citation: Ws. Oetting et al., MUTATIONS AND POLYMORPHISMS OF THE HUMAN P-GENE ASSOCIATED WITH P-RELATED OCULOCUTANEOUS ALBINISM (OCA2), American journal of human genetics, 57(4), 1995, pp. 1432-1432
A GENE CAUSING HERMANSKY-PUDLAK SYNDROME IN A PUERTO-RICAN POPULATIONMAPS TO CHROMOSOME 10Q2
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
ANALYSIS OF TYROSINASE MUTATIONS ASSOCIATED WITH TYROSINASE-RELATED OCULOCUTANEOUS ALBINISM (OCA1)
Authors: OETTING WS KING RA
Citation: Ws. Oetting et Ra. King, ANALYSIS OF TYROSINASE MUTATIONS ASSOCIATED WITH TYROSINASE-RELATED OCULOCUTANEOUS ALBINISM (OCA1), Pigment cell research, 7(5), 1994, pp. 285-290
ANALYSIS OF TYROSINASE GENE-MUTATIONS USING DIRECT AUTOMATED INFRAREDFLUORESCENCE DNA-SEQUENCING OF AMPLIFIED EXONS
Authors: OETTING WS FRYER JP OOFUJI Y MIDDENDORF LR BRUMBAUGH JA SUMMERS CG KING RA
Citation: Ws. Oetting et al., ANALYSIS OF TYROSINASE GENE-MUTATIONS USING DIRECT AUTOMATED INFRAREDFLUORESCENCE DNA-SEQUENCING OF AMPLIFIED EXONS, Electrophoresis, 15(2), 1994, pp. 159-164
MOLECULAR-BASIS OF OCULOCUTANEOUS ALBINISM
Authors: OETTING WS KING RA
Citation: Ws. Oetting et Ra. King, MOLECULAR-BASIS OF OCULOCUTANEOUS ALBINISM, Journal of investigative dermatology, 103(5), 1994, pp. 190000131-190000136
MOLECULAR-BASIS OF TYPE-I (TYROSINASE-RELATED) OCULOCUTANEOUS ALBINISM - MUTATIONS AND POLYMORPHISMS OF THE HUMAN TYROSINASE GENE
Authors: OETTING WS KING RA
Citation: Ws. Oetting et Ra. King, MOLECULAR-BASIS OF TYPE-I (TYROSINASE-RELATED) OCULOCUTANEOUS ALBINISM - MUTATIONS AND POLYMORPHISMS OF THE HUMAN TYROSINASE GENE, Human mutation, 2(1), 1993, pp. 1-6
A DINUCLEOTIDE DELETION (-DELTA-GA115) IN THE TYROSINASE GENE RESPONSIBLE FOR TYPE-I-A (TYROSINASE NEGATIVE) OCULOCUTANEOUS ALBINISM IN A PAKISTANI INDIVIDUAL
Authors: OETTING WS FRYER JP KING RA
Citation: Ws. Oetting et al., A DINUCLEOTIDE DELETION (-DELTA-GA115) IN THE TYROSINASE GENE RESPONSIBLE FOR TYPE-I-A (TYROSINASE NEGATIVE) OCULOCUTANEOUS ALBINISM IN A PAKISTANI INDIVIDUAL, Human molecular genetics, 2(7), 1993, pp. 1047-1048
EVOLUTION OF THE TYROSINASE-RELATED GENE (TYRL) IN PRIMATES
Authors: OETTING WS STINE OC TOWNSEND D KING RA
Citation: Ws. Oetting et al., EVOLUTION OF THE TYROSINASE-RELATED GENE (TYRL) IN PRIMATES, Pigment cell research, 6(3), 1993, pp. 171-177
UNUSUAL TRYOSINASE MUTATIONS ASSOCIATED WITH OCA1
Authors: OETTING WS SKACH W FRYER JP KING RA
Citation: Ws. Oetting et al., UNUSUAL TRYOSINASE MUTATIONS ASSOCIATED WITH OCA1, American journal of human genetics, 53(3), 1993, pp. 935-935
Risultati: 1-23 |