Frequent association of 22q11.2 deletion with tetralogy of Fallot

American Journal of Medical Genetics

Volumn 92, Issue 4, 2000, Pages 269-272

  Maeda, Jun ^a   Yamagishi, Hiroyuki ^a   Matsuoka, Rumiko ^b   Ishihara, Jun ^a   Tokumura, Mitsuaki ^a   Fukushima, Hiroyuki ^a   Ueda, Hideaki ^a   Takahashi, Etsuro ^a   Yoshiba, Shigeki ^a   Kojima, Yoshifumi ^a  

^a KEIO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b TOKYO WOMEN'S MEDICAL UNIVERSITY   (Japan)

Author keywords

2q11.2 deletion; Bronchomalacia; Chromosome; Major aortico pulmonary collateral arteries; Tetralogy of Fallot

Indexed keywords

ARTICLE; BRONCHOMALACIA; CHILD; CHROMOSOME 22Q; CHROMOSOME DELETION; DISEASE ASSOCIATION; FALLOT TETRALOGY; FEMALE; HUMAN; JAPAN; LUNG ATRESIA; MAJOR CLINICAL STUDY; MALE; PATENT DUCTUS ARTERIOSUS; PREVALENCE; PRIORITY JOURNAL; PULMONARY ARTERY; PULMONARY VALVE STENOSIS;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; DUCTUS ARTERIOSUS, PATENT; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; INFANT, NEWBORN; MALE; PULMONARY ARTERY; PULMONARY ATRESIA; PULMONARY VALVE STENOSIS; TETRALOGY OF FALLOT;

EID: 17144468115     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(20000605)92:4<269::AID-AJMG9>3.0.CO;2-L     Document Type: Article

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