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Results: 1-7 |
Results: 7
LINKAGE DISEQUILIBRIUM ANALYSIS IN A RECENTLY FOUNDED POPULATION - EVALUATION OF THE VARIEGATE PORPHYRIA FOUNDER IN SOUTH-AFRICAN AFRIKANERS
Authors: GROENEWALD JZ LIEBENBERG J GROENEWALD IM WARNICH L
Citation: Jz. Groenewald et al., LINKAGE DISEQUILIBRIUM ANALYSIS IN A RECENTLY FOUNDED POPULATION - EVALUATION OF THE VARIEGATE PORPHYRIA FOUNDER IN SOUTH-AFRICAN AFRIKANERS, American journal of human genetics, 62(5), 1998, pp. 1254-1258
MOLECULAR ANALYSIS REVEALS A HIGH MUTATION FREQUENCY IN THE FIRST UNTRANSLATED EXON OF THE PPOX GENE AND LARGELY EXCLUDES VARIEGATE PORPHYRIA IN A SUBSET OF CLINICALLY AFFECTED AFRIKANER FAMILIES
Authors: KOTZE MJ DEVILLIERS JNP GROENEWALD JZ ROONEY RN LOUBSER O THIART R OOSTHUIZEN CJJ VANNIEKERK MM GROENEWALD IM RETIEF AE WARNICH L
Citation: Mj. Kotze et al., MOLECULAR ANALYSIS REVEALS A HIGH MUTATION FREQUENCY IN THE FIRST UNTRANSLATED EXON OF THE PPOX GENE AND LARGELY EXCLUDES VARIEGATE PORPHYRIA IN A SUBSET OF CLINICALLY AFFECTED AFRIKANER FAMILIES, Molecular and cellular probes, 12(5), 1998, pp. 293-300
IDENTIFICATION OF 3 MUTATIONS AND ASSOCIATED HAPLOTYPES IN THE PROTOPORPHYRINOGEN OXIDASE GENE IN SOUTH-AFRICAN FAMILIES WITH VARIEGATE PORPHYRIA
Authors: WARNICH L KOTZE MJ GROENEWALD IM GROENEWALD JZ VANBRAKEL MG VANHEERDEN CJ DEVILLIERS JNP VANDEVEN WJM SCHOENMAKERS EFPM TAKETANI S RETIEF AE
Citation: L. Warnich et al., IDENTIFICATION OF 3 MUTATIONS AND ASSOCIATED HAPLOTYPES IN THE PROTOPORPHYRINOGEN OXIDASE GENE IN SOUTH-AFRICAN FAMILIES WITH VARIEGATE PORPHYRIA, Human molecular genetics, 5(7), 1996, pp. 981-984
MAPPING OF THE VARIEGATE PORPHYRIA (VP) GENE - CONTRADICTORY EVIDENCEFOR LINKAGE BETWEEN VP AND MICROSATELLITE MARKERS AT CHROMOSOME 14Q32
Authors: WARNICH L MEISSNER PN HIFT RJ LOUW JH VANHEERDEN CJ RETIEF AE
Citation: L. Warnich et al., MAPPING OF THE VARIEGATE PORPHYRIA (VP) GENE - CONTRADICTORY EVIDENCEFOR LINKAGE BETWEEN VP AND MICROSATELLITE MARKERS AT CHROMOSOME 14Q32, Human genetics, 97(5), 1996, pp. 690-692
2 NOVEL POINT MUTATIONS CAUSING RECEPTOR-NEGATIVE FAMILIAL HYPERCHOLESTEROLEMIA IN A SOUTH-AFRICAN INDIAN HOMOZYGOTE
Authors: LANGENHOVEN E WARNICH L THIART R RUBINSZTEIN DC VANDERWESTHUYZEN DR MARAIS AD KOTZE MJ
Citation: E. Langenhoven et al., 2 NOVEL POINT MUTATIONS CAUSING RECEPTOR-NEGATIVE FAMILIAL HYPERCHOLESTEROLEMIA IN A SOUTH-AFRICAN INDIAN HOMOZYGOTE, Atherosclerosis, 125(1), 1996, pp. 111-119
DINUCLEOTIDE REPEAT POLYMORPHISM AT THE D5S99 LOCUS ON CHROMOSOME 5Q33-34
Authors: GROENEWALD IM WARNICH L RETIEF AE
Citation: Im. Groenewald et al., DINUCLEOTIDE REPEAT POLYMORPHISM AT THE D5S99 LOCUS ON CHROMOSOME 5Q33-34, Human genetics, 96(4), 1995, pp. 497-499
A MICROSATELLITE-BASED INDEX MAP OF HUMAN CHROMOSOME-11
Authors: LITT M KRAMER P HAUGE XY WEBER JL WANG Z WILKIE PJ HOLT MS MISHRA S DONISKELLER H WARNICH L RETIEF AE JONES C WEISSENBACH J
Citation: M. Litt et al., A MICROSATELLITE-BASED INDEX MAP OF HUMAN CHROMOSOME-11, Human molecular genetics, 2(7), 1993, pp. 909-913
Risultati: 1-7 |