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Genetic mapping of gray leaf spot (GLS) resistance genes in maize

Theoretical and applied genetics, 2001-10, Vol.103 (5), p.797-803

2001

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Zircon ion microprobe studies bearing on the age and evolution of the Witwatersrand triad

Precambrian research, 1991-11, Vol.53 (3), p.243-266

1991

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Identification of Three Mutations and Associated Haplotypes in the Protoporphyrinogen Oxidase Gene in South African Families with Variegate Porphyria

Human molecular genetics, 1996-07, Vol.5 (7), p.981-984

1996

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The molecular basis and diagnosis of familial hypercholesterolaemia in South African Afrikaners

Annals of human genetics, 1991-05, Vol.55 (2), p.115-121

1991

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Detection of a frequent polymorphism in exon 10 of the low-density lipoprotein receptor gene

Human genetics, 1992-05, Vol.89 (3), p.362-362

1992

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A RFLP associated with the low-density lipoprotein receptor gene (LDLR)

Nucleic acids research, 1987-01, Vol.15 (1), p.376-376

1987

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A microsatellite-based index map of human chromosome 11

Human molecular genetics, 1993-07, Vol.2 (7), p.909-913

1993

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Highly informative dinucleotide repeat polymorphism at the D11S29 locus on chromosome 11q23

Human genetics, 1992-05, Vol.89 (3), p.357-359

1992

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Regional chromosome mapping of human collagen genes alpha 2(I) and alpha 1(I) (COLIA2 and COLIA1)

Human genetics, 1985-01, Vol.69 (4), p.304-308

1985

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Ring chromosome 15 in a patient with features of Fryns' syndrome

Journal of medical genetics, 1989-07, Vol.26 (7), p.469-470

1989

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Haplotypes identified by 10 DNA restriction fragment length polymorphisms at the human low density lipoprotein receptor gene locus

Journal of medical genetics, 1989-04, Vol.26 (4), p.255-259

1989

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Chromosome studies in 496 infertile males with a sperm count below 10 million/ml

Human genetics, 1984-01, Vol.66 (2-3), p.162-164

1984

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DNA screening of hyperlipidemic Afrikaners for familial hypercholesterolemia

Clinical genetics, 1992-07, Vol.42 (1), p.43-46

1992

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The frequency of the delta F508 mutation in the cystic fibrosis genes of 71 unrelated South African cystic fibrosis patients

South African medical journal, 1992-07, Vol.82 (1), p.13-15

1992

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Dinucleotide repeat polymorphism at the D5S99 locus on chromosome 5q33-34

Human genetics, 1995-10, Vol.96 (4), p.497-499

1995

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Mapping of the variegate porphyria (VP) gene : contradictory evidence for linkage between VP and microsatellite markers at chromosome 14q32

Human genetics, 1996-05, Vol.97 (5), p.690-692

1996

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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, 1998-10, Vol.12 (5), p.293-300

1998

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Improved visualization of the Bst EII RFLP of the human LDL receptor gene by co-digestion

Nucleic acids research, 1987-12, Vol.15 (23), p.10067-10067

1987

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An anonymous DNA probe (H38) [D10S37] detects a Msp I polymorphism on chromosome 10

Nucleic acids research, 1989-01, Vol.17 (1), p.474-474

1989

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The use of DNA markers in the pre-clinical diagnosis of familial adenomatous polyposis in families in South Africa

South African medical journal, 1995-04, Vol.85 (4), p.269-271

1995

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Deletion mapping of 39 random isolated Y-chromosome DNA fragments

Human genetics, 1990-07, Vol.85 (2), p.205-210

1990

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An anonymous human single copy genomic clone, D11S29 (L7) at 11q23, identifies a moderately frequent RFLP

Nucleic acids research, 1986-02, Vol.14 (4), p.1920-1920

1986

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Confirmation of a balanced chromosomal translocation using molecular techniques

Prenatal diagnosis, 1989-07, Vol.9 (7), p.505-513

1989

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RFLP detected by the anonymous DNA segment E88 (D2S17) assigned to chromosome 2

Nucleic acids research, 1987-07, Vol.15 (14), p.5908-5908

1987

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The identification of two low-density lipoprotein receptor gene mutations in South African familial hypercholesterolaemia

South African medical journal, 1989-10, Vol.76 (8), p.399-401

1989

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Genetic mapping of gray leaf spot (GLS) resistance genes in maize

Zircon ion microprobe studies bearing on the age and evolution of the Witwatersrand triad

Identification of Three Mutations and Associated Haplotypes in the Protoporphyrinogen Oxidase Gene in South African Families with Variegate Porphyria

The molecular basis and diagnosis of familial hypercholesterolaemia in South African Afrikaners

Detection of a frequent polymorphism in exon 10 of the low-density lipoprotein receptor gene

A RFLP associated with the low-density lipoprotein receptor gene (LDLR)

A microsatellite-based index map of human chromosome 11

Highly informative dinucleotide repeat polymorphism at the D11S29 locus on chromosome 11q23

Regional chromosome mapping of human collagen genes alpha 2(I) and alpha 1(I) (COLIA2 and COLIA1)

Ring chromosome 15 in a patient with features of Fryns' syndrome

Haplotypes identified by 10 DNA restriction fragment length polymorphisms at the human low density lipoprotein receptor gene locus

Chromosome studies in 496 infertile males with a sperm count below 10 million/ml

DNA screening of hyperlipidemic Afrikaners for familial hypercholesterolemia

The frequency of the delta F508 mutation in the cystic fibrosis genes of 71 unrelated South African cystic fibrosis patients

Dinucleotide repeat polymorphism at the D5S99 locus on chromosome 5q33-34

Mapping of the variegate porphyria (VP) gene : contradictory evidence for linkage between VP and microsatellite markers at chromosome 14q32

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

Improved visualization of the Bst EII RFLP of the human LDL receptor gene by co-digestion

An anonymous DNA probe (H38) [D10S37] detects a Msp I polymorphism on chromosome 10

The use of DNA markers in the pre-clinical diagnosis of familial adenomatous polyposis in families in South Africa

Deletion mapping of 39 random isolated Y-chromosome DNA fragments

An anonymous human single copy genomic clone, D11S29 (L7) at 11q23, identifies a moderately frequent RFLP

Confirmation of a balanced chromosomal translocation using molecular techniques

RFLP detected by the anonymous DNA segment E88 (D2S17) assigned to chromosome 2

The identification of two low-density lipoprotein receptor gene mutations in South African familial hypercholesterolaemia

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