Juvenile rheumatoid arthritis and del(22q11) syndrome: A non-random association

Journal of Medical Genetics

Volumn 35, Issue 11, 1998, Pages 943-947

  Verloes, Alain ^a   Curry, Cynthia ^b   Jamar, Mauricette ^a   Herens, Christian ^a   O'Lague, Patricia ^b   Marks, James ^b   Sarda, Pierre ^c   Blanchet, Patricia ^c  

^a UNIVERSITY OF LIÈGE   (Belgium)

^b UNIVERSITY OF CALIFORNIA   (United States)

^c HÔPITAL ARNAUD DE VILLENEUVE   (France)

Author keywords

del(22q11) syndrome; Juvenile rheumatoid arthritis

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CARPAL BONE; CASE REPORT; CHILD; CHROMOSOME 22Q; CHROMOSOME DELETION; CONGENITAL DEAFNESS; DEVELOPMENTAL DISORDER; DISEASE ASSOCIATION; DISEASE COURSE; FACE DYSMORPHIA; FALLOT TETRALOGY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GASTROESOPHAGEAL REFLUX; HUMAN; INTELLIGENCE; JUVENILE RHEUMATOID ARTHRITIS; MALE; MOTOR DYSFUNCTION; OSTEOLYSIS; OSTEOPENIA; PALATOPHARYNGEAL INCOMPETENCE; PRIORITY JOURNAL; PULMONARY ARTERY STENOSIS; SYNOSTOSIS; TARSAL BONE; TUBE FEEDING; WHEELCHAIR;

EID: 0031788096     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.35.11.943     Document Type: Article

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