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Mutation analysis of FGFR1‐3 in 11 Japanese patients with syndromic craniosynostoses
Authors:Akira Ohishi  Gen Nishimura  Fumiko Kato  Hiroyuki Ono  Kaori Maruwaka  Mako Ago  Hiroshi Suzumura  Etsuko Hirose  Yuki Uchida  Maki Fukami  Tsutomu Ogata
Affiliation:1. Department of Regional Neonatal‐Perinatal Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan;2. Department of Pediatrics, Hamamatsu University School of Medicine, Hamamatsu, Japan;3. Department of Radiology, Tokyo Metropolitan Children's Medical Center, Fuchu, Japan;4. Department of Pediatrics, Nagoya Daini Red Cross Hospital, Nagoya, Japan;5. Department of Neonatology, Tokyo Women's Medical University, Tokyo, Japan;6. Department of Pediatrics, Dokkyo Medical University School of Medicine, Tochigi, Japan;7. Department of Neonatology, Seirei‐Hamamatsu General Hospital, Hamamatsu, Japan;8. Department of Plastic, Reconstructive and Anesthetic Surgery, Chiba University School of Medicine, Chiba, Japan;9. Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan
Abstract:
Keywords:syndromic craniosynostosis  FGFR2  FGFR3  mutation
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