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A de novo interstitial deletion of 8p11.2 including ANK1 identified in a patient with spherocytosis, psychomotor developmental delay, and distinctive facial features

✍ Scribed by Kazushi Miya; Keiko Shimojima; Midori Sugawara; Shino Shimada; Hiroyuki Tsuri; Tomomi Harai-Tanaka; Sachiko Nakaoka; Hirokazu Kanegane; Toshio Miyawaki; Toshiyuki Yamamoto

Book ID: 116509004
Publisher: Elsevier Science
Year: 2012
Tongue: English
Weight: 384 KB
Volume: 506
Category: Article
ISSN: 0378-1119
DOI: 10.1016/j.gene.2012.06.086

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