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High frequencies of α -thalassaemia are the result of natural selection by malaria

Nature (London), 1986-06, Vol.321 (6072), p.744-750

1986

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Antibodies to glutamic acid decarboxylase are associated with HLA-DR genotypes in both Australians and Asians with type 1(insulin-dependent) diabetes mellitus

Diabetologia, 1992-10, Vol.35 (10), p.996-1001

1992

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An Asian-specific 9-bp deletion of mitochondrial DNA is frequently found in Polynesians

American journal of human genetics, 1989-04, Vol.44 (4), p.504-510

1989

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HLA-DR,DQ sequence polymorphisms in Polynesians, Micronesians, and Javanese

Human immunology, 1992-07, Vol.34 (3), p.153-161

1992

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Diversity in HLA-DR4-related DR,DQ haplotypes in Australia, Oceania, and China

Human immunology, 1991-12, Vol.32 (4), p.269-276

1991

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Variable gene usage of T cell receptor γ‐ and δ‐chain transcripts expressed in synovia and peripheral blood of patients with rheumatoid arthritis

Clinical and experimental immunology, 1992-02, Vol.87 (2), p.172-177

1992

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HLA class II diversity in Australian aborigines : unusual HLA-DRB1 alleles

Immunogenetics (New York), 1992-08, Vol.36 (5), p.333-337

1992

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C1 inhibitor functional deficiency in systemic lupus erythematosus (SLE)

Clinical and experimental immunology, 1993-05, Vol.92 (2), p.268-273

1993

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Evidence for oligoclonality of T cell receptor δ chain transcripts expressed in rheumatoid arthritis patients

European journal of immunology, 1992-10, Vol.22 (10), p.2587-2593

1992

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Restricted junctional diversity of T cell receptor δ gene rearrangements expressed in systemic lupus erythematosus (SLE) patients

Clinical and experimental immunology, 1994-09, Vol.97 (3), p.430-438

1994

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Analysis of T cell receptor Vα and Vβ gene usage in synovia of patients with rheumatoid arthritis

Immunology and cell biology, 1991-10, Vol.69 (5), p.349-354

1991

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A 3.5 kb deletion in the glycophorin C gene accounts for the Gerbich-negative blood group in Melanesians

Immunology and cell biology, 1994-02, Vol.72 (1), p.23-27

1994

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Prenatal diagnosis and successful intrauterine treatment of a female fetus with 21-hydroxylase deficiency

Medical journal of Australia, 1992-01, Vol.156 (2), p.132-135

1992

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Genetic Studies of Human Apolipoproteins. XVIII. Apolipoprotein Polymorphisms in Australian Aborigines

Human biology, 1991-04, Vol.63 (2), p.179-186

1991

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Characterization of Mutants of the Vitamin-D-Binding Protein/Group Specific Component: GC Aborigine (1A1) from Australian Aborigines and South African Blacks, and 2A9 from South Germany

Vox sanguinis, 1995-01, Vol.68 (1), p.50-54

1995

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Genetics of diabetes in Nauru: effects of foreign admixture, HLA antigens and the insulin-gene-linked polymorphism

Diabetologia, 1983-07, Vol.25 (1), p.13-17

1983

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The reasons for MHC polymorphism in man

Transplantation proceedings, 1989-02, Vol.21 (1 Pt 1), p.598

Serjeantson, S W

1989

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Strong association between the major histocompatibility complex and systemic lupus erythematosus in southern Chinese

Journal of rheumatology, 1987-12, Vol.14 (6), p.1128

1987

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HLA-DP variation as additional risk factor in IDDM

Diabetes (New York, N.Y.), 1990-07, Vol.39 (7), p.855-857

1990

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HLA-DRβ gene DNA polymorphisms revealed by Taq I correlate with HLA-DR specificities

Human immunology, 1986-03, Vol.15 (3), p.263-271

1986

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Persistence of γ δ T cell oligoclonality in the peripheral blood of rheumatoid arthritis patients

Immunology and cell biology, 1994-02, Vol.72 (1), p.7-11

1994

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Analysis of the Patterns of Inheritance of Splenomegaly and Serum IgM Levels in the Watut of Papua New Guinea

Human biology, 1991-04, Vol.63 (2), p.115-128

1991

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FcγRIIα: sequencing of the ligand binding domain in systemic lupus erythematosus patients

Clinical and experimental immunology, 1991-11, Vol.86 (2), p.199-202

1991

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Gm typing by immunoglobulin heavy-chain gene RFLP analysis

American journal of human genetics, 1988-08, Vol.43 (2), p.175-181

1988

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Strong association of HLA-DR3/DRw9 heterozygosity with early-onset insulin-dependent diabetes mellitus in Chinese

Diabetes (New York, N.Y.), 1987-11, Vol.36 (11), p.1297-1300

1987

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High frequencies of α -thalassaemia are the result of natural selection by malaria

Antibodies to glutamic acid decarboxylase are associated with HLA-DR genotypes in both Australians and Asians with type 1(insulin-dependent) diabetes mellitus

An Asian-specific 9-bp deletion of mitochondrial DNA is frequently found in Polynesians

HLA-DR,DQ sequence polymorphisms in Polynesians, Micronesians, and Javanese

Diversity in HLA-DR4-related DR,DQ haplotypes in Australia, Oceania, and China

Variable gene usage of T cell receptor γ‐ and δ‐chain transcripts expressed in synovia and peripheral blood of patients with rheumatoid arthritis

HLA class II diversity in Australian aborigines : unusual HLA-DRB1 alleles

C1 inhibitor functional deficiency in systemic lupus erythematosus (SLE)

Evidence for oligoclonality of T cell receptor δ chain transcripts expressed in rheumatoid arthritis patients

Restricted junctional diversity of T cell receptor δ gene rearrangements expressed in systemic lupus erythematosus (SLE) patients

Analysis of T cell receptor Vα and Vβ gene usage in synovia of patients with rheumatoid arthritis

A 3.5 kb deletion in the glycophorin C gene accounts for the Gerbich-negative blood group in Melanesians

Prenatal diagnosis and successful intrauterine treatment of a female fetus with 21-hydroxylase deficiency

Genetic Studies of Human Apolipoproteins. XVIII. Apolipoprotein Polymorphisms in Australian Aborigines

Characterization of Mutants of the Vitamin-D-Binding Protein/Group Specific Component: GC Aborigine (1A1) from Australian Aborigines and South African Blacks, and 2A9 from South Germany

Genetics of diabetes in Nauru: effects of foreign admixture, HLA antigens and the insulin-gene-linked polymorphism

The reasons for MHC polymorphism in man

Strong association between the major histocompatibility complex and systemic lupus erythematosus in southern Chinese

HLA-DP variation as additional risk factor in IDDM

HLA-DRβ gene DNA polymorphisms revealed by Taq I correlate with HLA-DR specificities

Persistence of γ δ T cell oligoclonality in the peripheral blood of rheumatoid arthritis patients

Analysis of the Patterns of Inheritance of Splenomegaly and Serum IgM Levels in the Watut of Papua New Guinea

FcγRIIα: sequencing of the ligand binding domain in systemic lupus erythematosus patients

Gm typing by immunoglobulin heavy-chain gene RFLP analysis

Strong association of HLA-DR3/DRw9 heterozygosity with early-onset insulin-dependent diabetes mellitus in Chinese

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