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 (Author), Sanders Merideth E (Author), Sahoo Trilochan (Author), Lalani Seema R (Author), Bejjani Bassem A (Author)
Format: Book
Published: BMC, 2006-02-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
Copy 1 Available