R. Harris

发表

Immunogenetic studies in families with rheumatoid arthritis and autoimmune thyroid disease.

D. Grennan, G. D. de Lange, P. Dyer, 1985, Journal of medical genetics.

Noonan Syndrome

M. Tassabehji, T. Strachan, N. Thakker, 2006 .

Detection, isolation and characterization of cell free HLA A and B antigens from human amniotic fluid.

P. Donnai, R. Harris, P. Klouda, 2008, Tissue antigens.

21-hydroxylase deficiency families with HLA identical affected and unaffected sibs.

T. Strachan, P. Sinnott, D. Price, 1989, Journal of medical genetics.

Genetics and biochemical variability of variants of 21 hydroxylase deficiency.

M. T. Gordon, D. Anderson, D. Conway, 1985, Journal of medical genetics.

STRONG ASSOCIATION BETWEEN IDIOPATHIC MEMBRANOUS NEPHROPATHY AND HLA-DRW3.

E. J. Acheson, J. Manos, N. Mallick, 1979, The Lancet.

Genetic factors in myasthenia gravis

R. Metcalfe, P. Dyer, R. Harris, 1988, Neurology.

A disease-associated germline deletion maps the type 2 neurofibromatosis (NF2) gene between the Ewing sarcoma region and the leukaemia inhibitory factor locus.

L. Gaunt, T. Strachan, R. Harris, 1993, Human molecular genetics.

Properdin factor B alleles in patients with idiopathic membranous nephropathy.

N. Mallick, P. Dyer, R. Harris, 2008, Tissue antigens.

HLA antigens associated with properdin factor B allotype BfF1.

P. Dyer, R. Harris, P. Klouda, 2008, Tissue antigens.

Pulsed field gel electrophoresis identifies a high degree of variability in the number of tandem 21‐hydroxylase and complement C4 gene repeats in 21‐hydroxylase deficiency haplotypes.

T. Strachan, P. Sinnott, S. Collier, 1989, The EMBO journal.

HLA haplotype sharing by siblings with rheumatoid arthritis: evidence for genetic heterogeneity.

D. Grennan, P. Dyer, P. Sanders, 1986, Annals of the rheumatic diseases.

Genetic variants of properdin factor B (Bf) in rheumatoid arthritis.

K. Walton, D. Grennan, P. Dyer, 1985, The Journal of rheumatology.

Clinical features, autoantibodies and HLA-DR antigens in rheumatoid arthritis.

K. Walton, D. Grennan, P. Dyer, 1985, The Journal of rheumatology.

Absence of linkage between adult polycystic kidney disease and the major histocompatibility system.

N. Mallick, P. Dyer, R. Harris, 2008, Tissue antigens.

Linkage and association between HLA and 21-hydroxylase deficiency.

D. Price, R. Harris, P. Klouda, 1980, Journal of medical genetics.

HLA AND CONGENITAL ADRENAL HYPERPLASIA

R. Harris, D. Price, K. Gelsthorpe, 1978, The Lancet.

HLA AND CONGENITAL ADRENAL HYPERPLASIA LINKAGE CONFIRMED

D. Price, R. Harris, P. Klouda, 1978, The Lancet.

Clinical and immunogenetic studies in multicase rheumatoid families.

D. Grennan, P. Dyer, R. Harris, 1984, The Quarterly journal of medicine.

Family studies in RA - the importance of HLA-DR4 and of genes for autoimmune thyroid disease.

D. Grennan, P. Dyer, R. Harris, 1983, The Journal of rheumatology.

Matching for properdin factor B (Bf) in renal transplantation.

A. Read, N. Mallick, P. Dyer, 1981, Transplantation.

Autoimmunity to native type II collagen--a distinct genetic subset of rheumatoid arthritis.

D. Grennan, P. Dyer, R. Harris, 1985, The Journal of rheumatology.

HLA antigens in patients with rheumatoid arthritis and antibodies to native type II collagen.

P. Holt, P. Dyer, R. Harris, 2008, Tissue antigens.

Genesis by meiotic unequal crossover of a de novo deletion that contributes to steroid 21-hydroxylase deficiency.

T. Strachan, C. Costigan, P. Sinnott, 1990, Proceedings of the National Academy of Sciences of the United States of America.