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Results: 1-12 |
Results: 12
HEREDITARY BUNDLE-BRANCH DEFECT - MAPPING REFINEMENT AND EVIDENCE FORHETEROGENEITY
Authors: CHEDID R STEPHAN E LOISELET J LEFRANC G BERGER G SAUER U VAKSMANN G VILLAIN E BLAYSAT G BRINK PA CORFIELD V BOUVAGNET P
Citation: R. Chedid et al., HEREDITARY BUNDLE-BRANCH DEFECT - MAPPING REFINEMENT AND EVIDENCE FORHETEROGENEITY, European journal of human genetics, 6, 1998, pp. 4222-4222
SUDDEN-DEATH DUE TO TROPONIN-T MUTATIONS
Authors: MOOLMAN JC CORFIELD VA POSEN B NGUMBELA K SEIDMAN C BRINK PA WATKINS H
Citation: Jc. Moolman et al., SUDDEN-DEATH DUE TO TROPONIN-T MUTATIONS, Journal of the American College of Cardiology, 29(3), 1997, pp. 549-555
MYOCARDIAL HYPERTROPHY .2. ROUND-TABLE DISCUSSION
Authors: BRINK PA NAIDOO DP MOTYER R GREGORY MA SEEDAT YK CASSIM S BRINK AJ DESAI DK
Citation: Pa. Brink et al., MYOCARDIAL HYPERTROPHY .2. ROUND-TABLE DISCUSSION, South African medical journal, 86, 1996, pp. 104-110
LEFT-VENTRICULAR HYPERTROPHY - IS WHAT IS GOOD FOR THE GOOSE GOOD FORTHE GANDER - AND, WHAT COMES FIRST - THE CHICKEN OR THE EGG
Authors: BRINK PA
Citation: Pa. Brink, LEFT-VENTRICULAR HYPERTROPHY - IS WHAT IS GOOD FOR THE GOOSE GOOD FORTHE GANDER - AND, WHAT COMES FIRST - THE CHICKEN OR THE EGG, South African medical journal, 86, 1996, pp. 5-6
MYOCARDIAL HYPERTROPHY .1. ROUND-TABLE DISCUSSION
Authors: BRINK AJ GREGORY MA CASSIM S NAIDOO DP BRINK PA SEEDAT YK MOTYER R
Citation: Aj. Brink et al., MYOCARDIAL HYPERTROPHY .1. ROUND-TABLE DISCUSSION, South African medical journal, 86, 1996, pp. 40-48
EVIDENCE OF A LONG QT FOUNDER GENE WITH VARYING PHENOTYPIC-EXPRESSIONIN SOUTH-AFRICAN FAMILIES
Authors: DEJAGER T CORBETT CH BADENHORST CW BRINK PA CORFIELD VA
Citation: T. Dejager et al., EVIDENCE OF A LONG QT FOUNDER GENE WITH VARYING PHENOTYPIC-EXPRESSIONIN SOUTH-AFRICAN FAMILIES, Journal of Medical Genetics, 33(7), 1996, pp. 567-573
IDENTIFICATION OF A NOVEL ALAL97THR MUTATION IN EXON-21 OF THE BETA-MYOSIN HEAVY-CHAIN GENE IN HYPERTROPHIC CARDIOMYOPATHY
Authors: MOOLMAN JC BRINK PA CORFIELD VA
Citation: Jc. Moolman et al., IDENTIFICATION OF A NOVEL ALAL97THR MUTATION IN EXON-21 OF THE BETA-MYOSIN HEAVY-CHAIN GENE IN HYPERTROPHIC CARDIOMYOPATHY, Human mutation, 6(2), 1995, pp. 197-198
GENE FOR PROGRESSIVE FAMILIAL HEART-BLOCK TYPE-I MAPS TO CHROMOSOME 19Q13
Authors: BRINK PA FERREIRA A MOOLMAN JC WEYMAR HW VANDERMERWE PL CORFIELD VA
Citation: Pa. Brink et al., GENE FOR PROGRESSIVE FAMILIAL HEART-BLOCK TYPE-I MAPS TO CHROMOSOME 19Q13, Circulation, 91(6), 1995, pp. 1633-1640
CLINICAL AND PROGNOSTIC EVALUATION OF FAMILIAL HYPERTROPHIC CARDIOMYOPATHY IN 2 SOUTH-AFRICAN FAMILIES WITH DIFFERENT CARDIAC BETA-MYOSIN HEAVY-CHAIN GENE-MUTATIONS
Authors: POSEN BM MOOLMAN JC CORFIELD VA BRINK PA
Citation: Bm. Posen et al., CLINICAL AND PROGNOSTIC EVALUATION OF FAMILIAL HYPERTROPHIC CARDIOMYOPATHY IN 2 SOUTH-AFRICAN FAMILIES WITH DIFFERENT CARDIAC BETA-MYOSIN HEAVY-CHAIN GENE-MUTATIONS, British Heart Journal, 74(1), 1995, pp. 40-46
GENETIC-LINKAGE STUDIES OF PROGRESSIVE FAMILIAL HEART-BLOCK, A CARDIAC CONDUCTION DISORDER
Authors: BRINK PA MOOLMAN JC FERREIRA A DEJAGER T WEYMAR HW MARTELL RW TORRINGTON M VANDERMERWE PL CORFIELD VA
Citation: Pa. Brink et al., GENETIC-LINKAGE STUDIES OF PROGRESSIVE FAMILIAL HEART-BLOCK, A CARDIAC CONDUCTION DISORDER, South African journal of science, 90(4), 1994, pp. 236-240
IMPROVED QUANTIFICATION WITH VALIDATION OF MULTIPLE MESSENGER-RNA SPECIES BY POLYMERASE CHAIN-REACTION - APPLICATION TO HUMAN MYOCARDIAL CREATINE-KINASE-M AND CREATINE-KINASE-B
Authors: MA TS BRINK PA PERRYMAN B ROBERTS R
Citation: Ts. Ma et al., IMPROVED QUANTIFICATION WITH VALIDATION OF MULTIPLE MESSENGER-RNA SPECIES BY POLYMERASE CHAIN-REACTION - APPLICATION TO HUMAN MYOCARDIAL CREATINE-KINASE-M AND CREATINE-KINASE-B, Cardiovascular Research, 28(4), 1994, pp. 464-471
IDENTIFICATION OF A NEW MISSENSE MUTATION AT ARG403, A CPG MUTATION HOTSPOT, IN EXON-13 OF THE BETA-MYOSIN HEAVY-CHAIN GENE IN HYPERTROPHICCARDIOMYOPATHY
Authors: MOOLMAN JC BRINK PA CORFIELD VA
Citation: Jc. Moolman et al., IDENTIFICATION OF A NEW MISSENSE MUTATION AT ARG403, A CPG MUTATION HOTSPOT, IN EXON-13 OF THE BETA-MYOSIN HEAVY-CHAIN GENE IN HYPERTROPHICCARDIOMYOPATHY, Human molecular genetics, 2(10), 1993, pp. 1731-1732
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