Bronchomalacia associated with pulmonary atresia, ventricular septal defect and major aortopulmonary collateral arteries, and chromosome 22q11.2 deletion

Clinical Genetics

Volumn 62, Issue 3, 2002, Pages 214-219

  Yamagishi, Hiroyuki ^a   Maeda, J ^a   Higuchi, M ^a   Katada, Y ^a   Yamagishi, C ^a   Matsuo, N ^a   Kojima, Y ^a  

^a KEIO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

Bronchomalacia; Chromosome 22q11.2 deletion; Congenital heart disease; Major aortopulmonary collateral arteries; Respiratory distress

Indexed keywords

ANGIOCARDIOGRAPHY; AORTOPULMONARY SEPTAL DEFECT; ARTICLE; BRONCHOGRAPHY; BRONCHOMALACIA; CASE REPORT; CHROMOSOME 22Q; CHROMOSOME DELETION; COLLATERAL CIRCULATION; DISEASE ASSOCIATION; DISEASE SEVERITY; FIBEROPTIC BRONCHOSCOPY; HEART VENTRICLE SEPTUM DEFECT; HUMAN; INFANT; LUNG ATRESIA; MALE; MEDICAL RECORD; NUCLEAR MAGNETIC RESONANCE IMAGING; ONSET AGE; PATHOGENESIS; PRIORITY JOURNAL; PROGNOSIS; RESPIRATORY DISTRESS;

AIRWAY OBSTRUCTION; CHROMOSOMES, HUMAN, PAIR 22; COLLATERAL CIRCULATION; HEART SEPTAL DEFECTS, VENTRICULAR; HUMANS; INFANT; INFANT, NEWBORN; MALE; PULMONARY ATRESIA; SEQUENCE DELETION;

BRONCHUS;

EID: 0036766281     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1034/j.1399-0004.2002.620305.x     Document Type: Article

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