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A de novo deletion of 20q11.2–q12 in a boy presenting with abnormal hands and feet, retinal dysplasia, and intractable feeding difficulty

✍ Scribed by Yoko Hiraki; Akira Nishimura; Michiko Hayashidani; Yoshiko Terada; Gen Nishimura; Nobuhiko Okamoto; Sachiko Nishina; Yoshinori Tsurusaki; Hiroshi Doi; Hirotomo Saitsu; Noriko Miyake; Naomichi Matsumoto


Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
214 KB
Volume
155
Category
Article
ISSN
1552-4825

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