Interruption of the aortic arch associated with deletion of chromosome 22q11 is associated with a subarterial and doubly committed ventricular septal defect in Japanese patients

Cardiology in the Young

Volumn 9, Issue 5, 1999, Pages 463-467

  Momma, Kazuo ^a   Ando, Masahiko ^a   Matsuoka, Rumiko ^a   Joo, Kunitaka ^b  

^a TOKYO WOMEN'S MEDICAL UNIVERSITY   (Japan)

^b Kyuuhuu Koseinenkin Hospital   (Japan)

Author keywords

Absent muscular outlet septum; Chromosome 22q11 deletion; DiGeorge syndrome; Interruption of aortic arch

Indexed keywords

ADOLESCENT; ARTICLE; CHILD; CHROMOSOME 22; CHROMOSOME DELETION; CONGENITAL MALFORMATION; DIGEORGE SYNDROME; FEMALE; GENETICS; HEART SEPTUM DEFECT; HUMAN; INFANT; MALE; MULTIPLE MALFORMATION SYNDROME; THORACIC AORTA;

ABNORMALITIES, MULTIPLE; ADOLESCENT; AORTA, THORACIC; CHILD; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; DIGEORGE SYNDROME; FEMALE; HEART SEPTAL DEFECTS, VENTRICULAR; HUMANS; INFANT; MALE;

EID: 0033195710     PISSN: 10479511     EISSN: None     Source Type: Journal    
DOI: 10.1017/s1047951100005357     Document Type: Article

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