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3q29 interstitial microdeletion syndrome: An inherited case associated with cardiac defect and normal cognition

โœ Scribed by Feng Li; Emily C. Lisi; Elizabeth S. Wohler; Ada Hamosh; Denise A.S. Batista


Book ID
116433192
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
199 KB
Volume
52
Category
Article
ISSN
1769-7212

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## Abstract The screening of individuals with mild dysmorphic features and mental retardation using whole genome scanning technologies has resulted in the delineation of several previously unrecognized microdeletion syndromes. Microdeletion of 3q29 has been recently described as one such new syndro