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Results: 1-25 | 26-26
Results: 1-25/26
SNAPBACK SSCP ANALYSIS - ENGINEERED CONFORMATION CHANGES FOR THE RAPID TYPING OF KNOWN MUTATIONS
Authors: WILTON SD HONEYMAN K FLETCHER S LAING NG
Citation: Sd. Wilton et al., SNAPBACK SSCP ANALYSIS - ENGINEERED CONFORMATION CHANGES FOR THE RAPID TYPING OF KNOWN MUTATIONS, Human mutation, 11(3), 1998, pp. 252-258
ALTERNATIVE DYSTROPHIN GENE TRANSCRIPTS IN GOLDEN RETRIEVER MUSCULAR-DYSTROPHY
Authors: SCHATZBERG SJ ANDERSON LVB WILTON SD KORNEGAY JN MANN CJ SOLOMON GG SHARP NJH
Citation: Sj. Schatzberg et al., ALTERNATIVE DYSTROPHIN GENE TRANSCRIPTS IN GOLDEN RETRIEVER MUSCULAR-DYSTROPHY, Muscle & nerve, 21(8), 1998, pp. 991-998
AN INTERCHROMOSOMAL DUPLICATION WITHIN THE DYSTROPHIN GENE
Authors: WILTON SD DAVIS M LIM L HARKER N FABIAN V GOLDBLATT J LAING NG
Citation: Sd. Wilton et al., AN INTERCHROMOSOMAL DUPLICATION WITHIN THE DYSTROPHIN GENE, Brain pathology, 7(4), 1997, pp. 1118-1118
REVERTANT FIBERS - A POTENTIAL THERAPY DMD
Authors: WILTON SD HONEYMAN K LLOYD F KOLE R
Citation: Sd. Wilton et al., REVERTANT FIBERS - A POTENTIAL THERAPY DMD, Brain pathology, 7(4), 1997, pp. 1219-1219
APOE GENOTYPING OF ARCHIVAL SPECIMENS BY MULTIPLEX SSCP ANALYSIS
Authors: WILTON SD HONEYMAN K DAVIS M LIM L KELLOWAY L FABIAN V
Citation: Sd. Wilton et al., APOE GENOTYPING OF ARCHIVAL SPECIMENS BY MULTIPLEX SSCP ANALYSIS, Brain pathology, 7(4), 1997, pp. 1367-1367
DIAGNOSIS OF INHERITED MYOPATHIES BY MOLECULAR METHODS
Authors: JOHNSEN RD HARKER NA WILTON SD SILBERSTEIN EP LAING NG KAKULAS BA
Citation: Rd. Johnsen et al., DIAGNOSIS OF INHERITED MYOPATHIES BY MOLECULAR METHODS, Brain pathology, 7(4), 1997, pp. 1372-1372
REVERTANT FIBERS - A POSSIBLE GENETIC THERAPY FOR DUCHENNE MUSCULAR-DYSTROPHY
Authors: WILTON SD DYE DE BLECHYNDEN LM LAING NG
Citation: Sd. Wilton et al., REVERTANT FIBERS - A POSSIBLE GENETIC THERAPY FOR DUCHENNE MUSCULAR-DYSTROPHY, Neuromuscular disorders, 7(5), 1997, pp. 329-335
A SPLICE-SITE MUTATION CAUSING OVINE MCARDLES-DISEASE
Authors: TAN P ALLEN JG WILTON SD AKKARI PA HUXTABLE CR LAING NG
Citation: P. Tan et al., A SPLICE-SITE MUTATION CAUSING OVINE MCARDLES-DISEASE, Neuromuscular disorders, 7(5), 1997, pp. 336-342
BANDSTAB - A PCR-BASED ALTERNATIVE TO CLONING PCR PRODUCTS
Authors: WILTON SD LIM L DYE D LAING N
Citation: Sd. Wilton et al., BANDSTAB - A PCR-BASED ALTERNATIVE TO CLONING PCR PRODUCTS, BioTechniques, 22(4), 1997, pp. 642-645
CHARACTERIZATION OF THE ERYTHROCYTE SUPEROXIDE-DISMUTASE ALLOZYMES INTHE DEER CERVUS-ELAPHUS
Authors: HE K WILTON SD TATE ML MURPHY MP
Citation: K. He et al., CHARACTERIZATION OF THE ERYTHROCYTE SUPEROXIDE-DISMUTASE ALLOZYMES INTHE DEER CERVUS-ELAPHUS, Animal genetics, 28(4), 1997, pp. 299-301
DYSTROPHIN GENE TRANSCRIPTS SKIPPING THE MDX MUTATION
Authors: WILTON SD DYE DE LAING NG
Citation: Sd. Wilton et al., DYSTROPHIN GENE TRANSCRIPTS SKIPPING THE MDX MUTATION, Muscle & nerve, 20(6), 1997, pp. 728-734
CHARACTERIZATION OF THE CHICKEN CU,ZN SUPEROXIDE-DISMUTASE GENE
Authors: STANTON JL WILTON SD LAING NG
Citation: Jl. Stanton et al., CHARACTERIZATION OF THE CHICKEN CU,ZN SUPEROXIDE-DISMUTASE GENE, DNA sequence, 6(6), 1996, pp. 357-360
3 NOVEL MUTATIONS AND 2 VARIANTS IN THE GENE FOR CU ZN SUPEROXIDE-DISMUTASE IN FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS/
Authors: HOSLER BA NICHOLSON GA SAPP PC CHIN W ORRELL RW DEBELLEROCHE JS ESTEBAN J HAYWARD LJ MCKENNAYASEK D YEUNG L CHERRYSON AK DENCH JE WILTON SD LAING NG HORVITZ HR BROWN RH
Citation: Ba. Hosler et al., 3 NOVEL MUTATIONS AND 2 VARIANTS IN THE GENE FOR CU ZN SUPEROXIDE-DISMUTASE IN FAMILIAL AMYOTROPHIC-LATERAL-SCLEROSIS/, Neuromuscular disorders, 6(5), 1996, pp. 361-366
ASSIGNMENT OF THE HUMAN ALPHA-TROPOMYOSIN GENE TPM4 TO BAND 19P13.1 BY FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: WILTON SD LIM L DOROSZ SD GUNN HC EYRE HJ CALLEN DF LAING NG
Citation: Sd. Wilton et al., ASSIGNMENT OF THE HUMAN ALPHA-TROPOMYOSIN GENE TPM4 TO BAND 19P13.1 BY FLUORESCENCE IN-SITU HYBRIDIZATION, Cytogenetics and cell genetics, 72(4), 1996, pp. 294-296
APOLIPOPROTEIN-E GENOTYPING IN DIAGNOSIS OF ALZHEIMERS-DISEASE
Authors: KAKULAS BA WILTON SD FABIAN VA JONES TM
Citation: Ba. Kakulas et al., APOLIPOPROTEIN-E GENOTYPING IN DIAGNOSIS OF ALZHEIMERS-DISEASE, Lancet, 348(9025), 1996, pp. 483-483
ALZHEIMERS-DISEASE AND APOLIPOPROTEIN-E GENOTYPE IN WESTERN-AUSTRALIA- AN AUTOPSY-VERIFIED SERIES
Authors: FABIAN VA JONES TM WILTON SD DENCH JE DAVIS MR LIM L KAKULAS BA
Citation: Va. Fabian et al., ALZHEIMERS-DISEASE AND APOLIPOPROTEIN-E GENOTYPE IN WESTERN-AUSTRALIA- AN AUTOPSY-VERIFIED SERIES, Medical journal of Australia, 165(2), 1996, pp. 77-80
A MUTATION IN THE ALPHA-TROPOMYOSIN GENE TPM3 ASSOCIATED WITH AUTOSOMAL-DOMINANT NEMALINE MYOPATHY
Authors: LAING NG WILTON SD AKKARI PA DOROSZ S BOUNDY K KNEEBONE C BLUMBERGS P WHITE S WATKINS H LOVE DR HAAN E
Citation: Ng. Laing et al., A MUTATION IN THE ALPHA-TROPOMYOSIN GENE TPM3 ASSOCIATED WITH AUTOSOMAL-DOMINANT NEMALINE MYOPATHY, Nature genetics, 9(1), 1995, pp. 75-79
ASSIGNMENT OF THE HUMAN BETA-TROPOMYOSIN GENE (TPM2) TO BAND 9P13 BY FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: HUNT CCJ EYRE HJ AKKARI PA MEREDITH C DOROSZ SM WILTON SD CALLEN DF LAING NG BAKER E
Citation: Ccj. Hunt et al., ASSIGNMENT OF THE HUMAN BETA-TROPOMYOSIN GENE (TPM2) TO BAND 9P13 BY FLUORESCENCE IN-SITU HYBRIDIZATION, Cytogenetics and cell genetics, 71(1), 1995, pp. 94-95
ASSIGNMENT OF THE HUMAN SKELETAL-MUSCLE ALPHA-TROPOMYOSIN GENE (TPM1)TO BAND 15Q22 BY FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: EYRE H AKKARI PA WILTON SD CALLEN DC BAKER E LAING NG
Citation: H. Eyre et al., ASSIGNMENT OF THE HUMAN SKELETAL-MUSCLE ALPHA-TROPOMYOSIN GENE (TPM1)TO BAND 15Q22 BY FLUORESCENCE IN-SITU HYBRIDIZATION, Cytogenetics and cell genetics, 69(1-2), 1995, pp. 15-17
ASSIGNMENT OF THE HUMAN ALPHA-TROPOMYOSIN GENE TPM3 TO 1Q22-]Q23 BY FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: WILTON SD EYRE H AKKARI PA WATKINS HC MACRAE C LAING NG CALLEN DC
Citation: Sd. Wilton et al., ASSIGNMENT OF THE HUMAN ALPHA-TROPOMYOSIN GENE TPM3 TO 1Q22-]Q23 BY FLUORESCENCE IN-SITU HYBRIDIZATION, Cytogenetics and cell genetics, 68(1-2), 1995, pp. 122-124
AUTOSOMAL-DOMINANT DISTAL MYOPATHY - LINKAGE TO CHROMOSOME-14
Authors: LAING NG LAING BA MEREDITH C WILTON SD ROBBINS P HONEYMAN K DOROSZ S KOZMAN H MASTAGLIA FL KAKULAS BA
Citation: Ng. Laing et al., AUTOSOMAL-DOMINANT DISTAL MYOPATHY - LINKAGE TO CHROMOSOME-14, American journal of human genetics, 56(2), 1995, pp. 422-427
IDENTIFICATION OF A POINT MUTATION AND GERMINAL MOSAICISM IN A DUCHENNE MUSCULAR-DYSTROPHY FAMILY
Authors: WILTON SD CHANDLER DC KAKULAS BA LAING NG
Citation: Sd. Wilton et al., IDENTIFICATION OF A POINT MUTATION AND GERMINAL MOSAICISM IN A DUCHENNE MUSCULAR-DYSTROPHY FAMILY, Human mutation, 3(2), 1994, pp. 133-140
THE NEM1 AUTOSOMAL-DOMINANT NEMALINE MYOPATHY GENE LINKAGE REGION IS BETWEEN MFD215 AND APOA2
Authors: AKKARI PA BOUNDY K WHITE SJ WILTON SD LAING NG
Citation: Pa. Akkari et al., THE NEM1 AUTOSOMAL-DOMINANT NEMALINE MYOPATHY GENE LINKAGE REGION IS BETWEEN MFD215 AND APOA2, Cytogenetics and cell genetics, 67(3), 1994, pp. 166-166
ASSIGNMENT OF THE HUMAN SKELETAL-MUSCLE ALPHA ACTIN GENE (ACTA1) TO 1Q42 BY FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: AKKARI PA EYRE HJ WILTON SD CALLEN DF LANE SA MEREDITH C KEDES L LAING NG
Citation: Pa. Akkari et al., ASSIGNMENT OF THE HUMAN SKELETAL-MUSCLE ALPHA ACTIN GENE (ACTA1) TO 1Q42 BY FLUORESCENCE IN-SITU HYBRIDIZATION, Cytogenetics and cell genetics, 65(4), 1994, pp. 265-267
VERIFICATION OF CARRIER STATUS FOR BECKER MUSCULAR-DYSTROPHY FROM ANALYSIS OF A BLIGHTED OVUM
Authors: WILTON SD GOLDBLATT J LAING NG
Citation: Sd. Wilton et al., VERIFICATION OF CARRIER STATUS FOR BECKER MUSCULAR-DYSTROPHY FROM ANALYSIS OF A BLIGHTED OVUM, Prenatal diagnosis, 13(8), 1993, pp. 757-762
Risultati: 1-25 | 26-26