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Interstitial deletion of the short arm of chromosome 10 del(10)(p11.2p12.32) in a patient with congenital heart disease, minor dysmorphism, and mental retardation

✍ Scribed by Farkhondeh Behjati; Yousef Shafeghati; Kimia Kahrizi; Saghar Ghasemi Firouzabadi; Hossein Najmabadi; Neil Dixon; Angela F. Davies

Publisher: John Wiley and Sons
Year: 2008
Tongue: English
Weight: 117 KB
Volume: 146A
Category: Article
ISSN: 1552-4825
DOI: 10.1002/ajmg.a.32575

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