Bronchomalacia associated with pulmonary atresia, ventricular septal defect and major aortopulmonary collateral arteries, and chromosome 22q11.2 deletion-Reference-Cited by-同舟云学术

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

Published:2002-09 Issue:3 Volume:62 Page:214-219
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Yamagishi H,Maeda J,Higuchi M,Katada Y,Yamagishi C,Matsuo N,Kojima Y

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-0004.2002.620305.x/fullpdf

Reference27 articles.

1. Chromosome 22q11 monosomy and the genetic basis of congenital heart disease;Johnson;J Pediatr,1996

2. Tetralogy of Fallot with pulmonary atresia associated with chromosome 22q11 deletion;Momma;J Am Coll Cardiol,1996

3. Frequent association of 22q11.2 deletion with tetralogy of Fallot;Maeda;Am J Med Genet,2000

4. Pulmonary blood supply in patients with pulmonary atresia and ventricular septal defect;Liao;J Am Coll Cardiol,1985

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