The camptodactyly-arthropathy-coxa vara-pericarditis syndrome: Clinical features and genetic mapping to human chromosome 1

Arthritis and Rheumatism

Volumn 41, Issue 4, 1998, Pages 730-735

  Bahabri, Sultan A ^a   Suwairi, Wafaa M ^b,c   Laxer, Ronald M ^d   Polinkovsky, Alexander ^c   Dalaan, Abdullah A ^a   Warman, Matthew L ^e  

^a KING FAISAL SPECIALIST HOSPITAL AND RESEARCH CENTER   (Saudi Arabia)

^b Prince Sultan Military Medical City   (Saudi Arabia)

^c CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^d HOSPITAL FOR SICK CHILDREN   (Canada)

^e CASE WESTERN RESERVE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ARTHROPATHY; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CAMPTODACTYLY; CHILD; CHROMOSOME 1Q; CLINICAL ARTICLE; CONSANGUINEOUS MARRIAGE; COXA VARA; FEMALE; GENE LOCATION; GENE LOCUS; GENETIC SUSCEPTIBILITY; HUMAN; MALE; MARKER GENE; PERICARDITIS; PRIORITY JOURNAL;

ADOLESCENT; ANKLE JOINT; ARTHRITIS, JUVENILE RHEUMATOID; CHILD; CHILD, PRESCHOOL; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 1; CONTRACTURE; ELBOW JOINT; FEMALE; FINGER JOINT; FINGERS; GENETIC MARKERS; HIP; HIP JOINT; HOMOZYGOTE; HUMANS; KNEE JOINT; LOD SCORE; MALE; PEDIGREE; PERICARDITIS; SYNDROME; WRIST JOINT;

EID: 0031947369     PISSN: 00043591     EISSN: None     Source Type: Journal    
DOI: 10.1002/1529-0131(199804)41:4<730::AID-ART22>3.0.CO;2-Y     Document Type: Article

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