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
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]