Coarctation of the aorta and mild to moderate developmental delay in a child with a <it>de novo </it>deletion of chromosome 15(q21.1q22.2)

<p>Abstract</p> <p>Background</p> <p>Deletion of 15q21q22 is a rare chromosomal anomaly. To date, there have been nine reports describing ten individuals with different segmental losses involving 15q21 and 15q22. Many of these individuals have common features of growth...

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Bibliographic Details
Main Authors: Peters Sarika U, Sanders Merideth E, Sahoo Trilochan, Lalani Seema R, Bejjani Bassem A
Format: Article
Language:English
Published: BMC 2006-02-01
Series:BMC Medical Genetics
Online Access:http://www.biomedcentral.com/1471-2350/7/8