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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Format: | Book |
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BMC,
2006-02-01T00:00:00Z.
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A1234.567 |
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