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Publisher: Wiley-Blackwell

Volume 52, Number 4, 1 December 2012

Abstracts
pp. A1-A21(21)

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Announcement
pp. J5-J6(2)

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Professor Naomasa Okamoto, 1921–2012
pp. 185-185(1)
Author: Ikeda, Takayoshi

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Prenatal diagnosis of osteogenesis imperfecta type II by three‐dimensional computed tomography: The current state of fetal computed tomography
pp. 203-206(4)
Authors: Akizawa, Yoshika; Nishimura, Gen; Hasegawa, Tomonobu; Takagi, Masaki; Kawamichi, Yayoi; Matsuda, Yoshio; Matsui, Hideo; Saito, Kayoko

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Ehlers‐Danlos syndrome, vascular type: A novel missense mutation in the COL3A1 gene
pp. 207-210(4)
Authors: Masuno, Mitsuo; Watanabe, Atsushi; Naing, Banyar Than; Shimada, Takashi; Fujimoto, Wataru; Ninomiya, Shinsuke; Ueda, Yasunori; Kadota, Kazushige; Kotaka, Tatsuya; Kondo, Eisei; Yamanouchi, Yasuko; Inoue, Mika; Ouchi, Kazunobu; Kuroki, Yoshikazu

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Novel CRLF1 gene mutation in a newborn infant diagnosed with Crisponi syndrome
pp. 216-218(3)
Authors: Hakan, Nilay; Eminoglu, Fatma Tuba; Aydin, Mustafa; Zenciroglu, Aysegul; Karadag, Nazmiye Nilgun; Dursun, Arzu; Okumus, Nurullah; Ceylaner, Serdar

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Hepatoblastoma in an infant with paternal uniparental disomy 14
pp. 219-220(2)
Authors: Horii, Mariko; Horiuchi, Hiroko; Momoeda, Mikio; Nakagawa, Machiko; Hirata, Michio; Kusakawa, Isao; Yamanaka, Michiko

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Reviewers
pp. 221-222(2)

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