Chromosome 2p16.1-p15 deletion syndrome: Difference between revisions

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==Overview==
==Overview==


Chromosome 2p16.1-p15 Deletion Syndrome is a rare genetic disorder characterized by a range of manifestations including mental retardation and skull and facial anomalies.
Chromosome 2p16.1-p15 Deletion Syndrome is a rare genetic disorder characterized by a range of manifestations including mental retardation and skull and facial anomalies.<ref>http://www.omim.org/entry/612513</ref>


==References==
==References==

Latest revision as of 20:21, 11 August 2012

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Chromosome 2p16.1-p15 Deletion Syndrome is a rare genetic disorder characterized by a range of manifestations including mental retardation and skull and facial anomalies.[1]

References

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