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...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2006-02-01
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Series: | BMC Medical Genetics |
Online Access: | http://www.biomedcentral.com/1471-2350/7/8 |