Volume 11, Issue S1 pp. S18-S19
Mutation in Brief
Free Access

Two common mutations 934C to G and 937C to G of fibroblast growth factor receptor 2 (FGFR2) gene in Chinese patients with apert syndrome

Fuu-Jen Tsai

Corresponding Author

Fuu-Jen Tsai

Department of Pediatrics, China Medical College Hospital, Taichung, Taipei, Taiwan

Department of Pediatrics, China Medical College Hospital, Taichung, Taipei, Taiwan. Fax: 886-4-2032798Search for more papers by this author
Wuh-Liang Hwu

Wuh-Liang Hwu

Department of Pediatrics and Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan

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Shuan-Pei Lin

Shuan-Pei Lin

Department of Pediatrics, Mackay Memorial Hospital, Taipei, Taiwan

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Jan-Gowth Chang

Jan-Gowth Chang

Department of Molecular Medicine, Tapei Municipal Jen-Ai Hospital, Taipei, Taiwan

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Tso-Ren Wang

Tso-Ren Wang

Department of Pediatrics and Medical Genetics, National Taiwan University Hospital, Taipei, Taiwan

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Chang-Hai Tsai

Chang-Hai Tsai

Department of Pediatrics, China Medical College Hospital, Taichung, Taipei, Taiwan

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First published: 28 April 2011
Citations: 3
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