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Comparative trial of prednisone plus aspirin versus aspirin alone in the treatment of anticardiolipin antibody-positive obstetric patients

American journal of obstetrics and gynecology, 1993-12, Vol.169 (6), p.1411-1417

1993

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The molecular basis of C6 deficiency in the western Cape, South Africa

Human genetics, 1998-10, Vol.103 (4), p.506-512

1998

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Complement C7 deficiency : seven further molecular defects and their associated marker haplotypes

Human genetics, 1998-10, Vol.103 (4), p.513-519

1998

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C7 deficiency in an Irish family: a deletion defect which is predominant in the Irish

Clinical and experimental immunology, 1998-12, Vol.114 (3), p.355-361

1998

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A physical map of the C6 and C7 complement component gene region on chromosome 5p13

Human molecular genetics, 1993-07, Vol.2 (7), p.1035-1036

1993

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Structure of the human C6 gene

Biochemistry (Easton), 1993-06, Vol.32 (24), p.6198-6205

1993

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An unusual combined insertion/deletion polymorphism in intron 10 of the human complement C6 gene

Human genetics, 1997-07, Vol.100 (1), p.104-108

1997

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Correlation of a Glu/Ala substitution at position 98 with the complement C6 A/B phenotypes

Human molecular genetics, 1993-05, Vol.2 (5), p.591-592

1993

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Difficulties in the ascertainment of C9 deficiency: lessons to be drawn from a compound heterozygote C9‐deficient subject

Clinical and experimental immunology, 1997-06, Vol.108 (3), p.500-506

1997

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DNA haplotypes of the complement C6 and C7 genes associated with deficiencies of the seventh component; and a new DNA polymorphism in C7 exon 13

Annals of human genetics, 1997-07, Vol.61 (4), p.287-298, Article S0003480097006234

1997

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DNA polymorphisms of the complement C6 and C7 genes

Annals of human genetics, 1995-04, Vol.59 (2), p.163-181

1995

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Evolution of the Terminal Complement Genes: Ancient and Modern

Experimental and clinical immunogenetics, 1998-01, Vol.15 (4), p.235-243

Hobart, M.J.

1998

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Complement component C6 and C7 haplotypes associated with deficiencies of C6

Annals of human genetics, 1995-04, Vol.59 (2), p.183-195

1995

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C6 epitope expression by an unrelated antisense cDNA clone: an inadvertent surface-simulation mimotope

Proceedings of the Royal Society. B, Biological sciences, 1993-05, Vol.252 (1334), p.157-162

1993

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C6 haplotypes: associations of a Dde I site polymorphism to complement deficiency genes and the Msp I restriction fragment length polymorphism (RFLP)

Clinical and experimental immunology, 1994-02, Vol.95 (2), p.351-356

1994

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How partial C7 deficiency with chronic and recurrent bacterial infections can mimic total C7 deficiency: temporary restoration of host C7 levels following plasma transfusion

Immunology, 1996-07, Vol.88 (3), p.407-411

1996

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Physical linkage and orientation of the human complement C8α and C8β genes on chromosome 1p32

Human genetics, 1996-10, Vol.98 (4), p.443-446

1996

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Structure of the human C7 gene and comparison with the C6, C8A, C8B, and C9 genes

The Journal of immunology (1950), 1995-05, Vol.154 (10), p.5188-5194

1995

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Post-term Pregnancy

Clinics in perinatology, 1989-12, Vol.16 (4), p.909-915

Hobart, John M.

1989

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Importance of the third thrombospondin repeat of C6 for terminal complement complex assembly

Immunology, 1995-06, Vol.85 (2), p.214-219

1995

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Midtrimester Rh sensitization associated with circulating anticardiolipin antibodies and elevated maternal serum alpha-fetoprotein. A case report

Journal of reproductive medicine, 1995-06, Vol.40 (6), p.477

1995

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A cleavable biotinylating agent and its use in protein electroblots

Journal of immunological methods, 1992-08, Vol.153 (1), p.93-98

1992

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A novel protein polymorphism of human complement C7 detected by a monoclonal antibody

Immunogenetics (New York), 1992-04, Vol.35 (6), p.398-402

1992

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Phenotypic genetics of complement components

Philosophical transactions of the Royal Society of London. Series B, Biological sciences, 1984-09, Vol.306 (1129), p.325-331

Hobart, M J

1984

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Reference Typing Report for Complement Components C6, C7 and C9 Including Mutations Leading to Deficiencies

Experimental and clinical immunogenetics, 1998-01, Vol.15 (4), p.268-285

1998

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Comparative trial of prednisone plus aspirin versus aspirin alone in the treatment of anticardiolipin antibody-positive obstetric patients

The molecular basis of C6 deficiency in the western Cape, South Africa

Complement C7 deficiency : seven further molecular defects and their associated marker haplotypes

C7 deficiency in an Irish family: a deletion defect which is predominant in the Irish

A physical map of the C6 and C7 complement component gene region on chromosome 5p13

Structure of the human C6 gene

An unusual combined insertion/deletion polymorphism in intron 10 of the human complement C6 gene

Correlation of a Glu/Ala substitution at position 98 with the complement C6 A/B phenotypes

Difficulties in the ascertainment of C9 deficiency: lessons to be drawn from a compound heterozygote C9‐deficient subject

DNA haplotypes of the complement C6 and C7 genes associated with deficiencies of the seventh component; and a new DNA polymorphism in C7 exon 13

DNA polymorphisms of the complement C6 and C7 genes

Evolution of the Terminal Complement Genes: Ancient and Modern

Complement component C6 and C7 haplotypes associated with deficiencies of C6

C6 epitope expression by an unrelated antisense cDNA clone: an inadvertent surface-simulation mimotope

C6 haplotypes: associations of a Dde I site polymorphism to complement deficiency genes and the Msp I restriction fragment length polymorphism (RFLP)

How partial C7 deficiency with chronic and recurrent bacterial infections can mimic total C7 deficiency: temporary restoration of host C7 levels following plasma transfusion

Physical linkage and orientation of the human complement C8α and C8β genes on chromosome 1p32

Structure of the human C7 gene and comparison with the C6, C8A, C8B, and C9 genes

Post-term Pregnancy

Importance of the third thrombospondin repeat of C6 for terminal complement complex assembly

Midtrimester Rh sensitization associated with circulating anticardiolipin antibodies and elevated maternal serum alpha-fetoprotein. A case report

A cleavable biotinylating agent and its use in protein electroblots

A novel protein polymorphism of human complement C7 detected by a monoclonal antibody

Phenotypic genetics of complement components

Reference Typing Report for Complement Components C6, C7 and C9 Including Mutations Leading to Deficiencies

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