Congenital Anomalies

Cover image for Vol. 57 Issue 1

Edited By: Yuji Nakajima

Impact Factor: 0.985

ISI Journal Citation Reports © Ranking: 2015: 91/120 (Pediatrics)

Online ISSN: 1741-4520

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    Dynamics of gyrification in the human cerebral cortex during development (pages 8–14)

    Ririko Yoshida, Koichi Ishizu, Shigehito Yamada, Chigako Uwabe, Tomohisa Okada, Kaori Togashi and Tetsuya Takakuwa

    Version of Record online: 4 JAN 2017 | DOI: 10.1111/cga.12179

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    Cartilage-hair hypoplasia associated with isolated hypoganglionosis: A case report (pages 32–34)

    Yoshitomo Yasui, Miyuki Kohno, Syouichi Nishida, Tsubasa Shironomae, Miwa Satomi, Tsuyoshi Kuwahara, Sadayoshi Takahashi and Yo Niida

    Version of Record online: 4 JAN 2017 | DOI: 10.1111/cga.12175

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    Exome sequencing identifies a novel nonsense mutation of HOXD13 in a Chinese family with synpolydactyly (pages 4–7)

    Bo Wang, Niu Li, Juan Geng, Zhigang Wang, Qihua Fu, Jian Wang and Yunlan Xu

    Version of Record online: 4 JAN 2017 | DOI: 10.1111/cga.12173

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    Evaluation of the maxillofacial morphological characteristics of Apert syndrome infants (pages 15–23)

    Hitomi Kakutani, Yoshiaki Sato, Yuri Tsukamoto-Takakusagi, Fumio Saito, Akihiko Oyama and Junichiro Iida

    Version of Record online: 4 JAN 2017 | DOI: 10.1111/cga.12180

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    Foxc2CreERT2 knock-in mice mark stage-specific Foxc2-expressing cells during mouse organogenesis (pages 24–31)

    Mohammed Badrul Amin, Naoyuki Miura, Mohammad Khaja Mafij Uddin, Mohammod Johirul Islam, Nobuaki Yoshida, Sachiko Iseki, Tsutomu Kume, Paul A. Trainor, Hirotomo Saitsu and Kazushi Aoto

    Version of Record online: 4 JAN 2017 | DOI: 10.1111/cga.12198

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