Frequency of 22q11.2 microdeletion in children with congenital heart defects in western poland
<p>Abstract</p> <p>Background</p> <p>The 22q11.2 microdeletion syndrome (22q11.2 deletion syndrome -22q11.2DS) refers to congenital abnormalities, including primarily heart defects and facial dysmorphy, thymic hypoplasia, cleft palate and hypocalcaemia. Microdeletion wi...
Main Authors: | , , , , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2010-12-01
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Series: | BMC Pediatrics |
Online Access: | http://www.biomedcentral.com/1471-2431/10/88 |