Microdeletion of chromosomal region 22q11 in DiGeorge syndrome: report of a case.

Abstract

This is a case of chromosome 22q11 deletion in a female Chinese infant with DiGeorge syndrome. Cardiac anomalies included a type B interrupted aortic arch from the descending aorta with an aberrant right subclavian artery, a large ventricular septal defect, a small atrial septal defect and a large patent ductus arteriosus. This patient was small for her age… (More)

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Cite this paper

@article{Hou1995MicrodeletionOC, title={Microdeletion of chromosomal region 22q11 in DiGeorge syndrome: report of a case.}, author={Jianhua Hou and J. K. Wang and C. C. Chou and Tongwen Wang}, journal={Journal of the Formosan Medical Association = Taiwan yi zhi}, year={1995}, volume={94 4}, pages={200-2} }