Interrupted aortic arch type C associated with DiGeorge syndrome in 22q11.2 deletion: First case detected in Japan

Pediatrics International

Volumn 47, Issue 6, 2005, Pages 698-700

  Fujii, Isao ^a,b   Ueno, Yasushi ^a   Kurano, Ryouichi ^a   Goto, Yoshitaka ^a  

^a KUMAMOTO REGIONAL MEDICAL CENTER   (Japan)

^b SOJO UNIVERSITY   (Japan)

Author keywords

22q11.2 deletion; Autopsy case; DiGeorge syndrome; Interrupted aortic arch type C

Indexed keywords

AORTA ARCH ANOMALY; ARTICLE; AUTOPSY; CASE REPORT; CHROMOSOME ANALYSIS; CHROMOSOME DELETION; CHROMOSOME DELETION 22Q11.2; CLINICAL FEATURE; DIGEORGE SYNDROME; DISEASE ASSOCIATION; HEART VENTRICLE SEPTUM DEFECT; HEMIZYGOSITY; HUMAN; HUMAN TISSUE; IN SITU HYBRIDIZATION; JAPAN; MALE; NEWBORN; PRIORITY JOURNAL; SYMPTOMATOLOGY; CHROMOSOME 22; CONGENITAL MALFORMATION; GENETICS; THORACIC AORTA;

AORTA, THORACIC; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; DIGEORGE SYNDROME; HUMANS; INFANT, NEWBORN; JAPAN; MALE;

EID: 33644876735     PISSN: 13288067     EISSN: 1442200X     Source Type: Journal    
DOI: 10.1111/j.1442-200x.2005.02148.x     Document Type: Article

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