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Identification of a novel frameshift mutation (383insT) in theRUNX2(PEBP2 α/CBFA1/AML3) gene in a Japanese patient with cleidocranial dysplasia

✍ Scribed by Masae Goseki-Sone; Hideo Orimo; Atsushi Watanabe; Ryoko Hamatani; Masahiko Yokozeki; Kimie Ohyama; Takayuki Kuroda; Hisashi Watanabe; Hidetaka Miyazaki; Takashi Shimada; Shinichiro Oida

Book ID: 106231521
Publisher: Springer
Year: 2001
Tongue: English
Weight: 370 KB
Volume: 19
Category: Article
ISSN: 0914-8779
DOI: 10.1007/s007740170030

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