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Volumn 46, Issue 1, 2002, Pages 75-82

Association of familial and sporadic rheumatoid arthritis with a single corticotropin-releasing hormone genomic region (8q12.3) haplotype

(13) Fife, Mark a Steer, Sophia a Fisher, Sheila a Newton, Julia b McKay, Kirsten b Worthington, Jane c Shah, Chandrabala a Polley, Andreas d Rosenthal, Andre d Ollier, William c Lewis, Cathryn a Wordsworth, Paul b Lanchbury, Jerry a,e

a KING'S COLLEGE LONDON (United Kingdom)

b UNIVERSITY OF OXFORD (United Kingdom)

c UNIVERSITY OF MANCHESTER (United Kingdom)

d FRITZ LIPMANN INSTITUTE (Germany)

e GUY S HOSPITAL (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CORTICOTROPIN RELEASING FACTOR;

ARTICLE; CHROMOSOME 8Q; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENETIC LINKAGE; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; PRIORITY JOURNAL; RHEUMATOID ARTHRITIS;

ARTHRITIS, RHEUMATOID; CHROMOSOMES, HUMAN, PAIR 8; CORTICOTROPIN-RELEASING HORMONE; FAMILY HEALTH; GENE FREQUENCY; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HUMANS; POLYMORPHISM, GENETIC; TANDEM REPEAT SEQUENCES;

EID: 0036161902 PISSN: 00043591 EISSN: None Source Type: Journal
DOI: 10.1002/1529-0131(200201)46:1<75::AID-ART10034>3.0.CO;2-3 Document Type: Article

Times cited : (21)

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