Somatic FGFR and TWIST Mutations are not a Common Cause of Isolated Nonsyndromic Single Suture Craniosynostosis
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概要
- 論文の詳細を見る
- 2007-03-01
著者
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DAVID David
Australian Craniofacial Unit, Women and Children's Hospital, and the University of Adelaide
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Anderson Peter
Australian Craniofacial Unit Women's And Children's Hospital
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COX Timothy
Australian Craniofacial Institute, associated with the University of Adelaide
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ROSCIOLI Tony
South Eastern Area Laboratory Service, Molecular and Cytogenetics laboratory, Prince of Wales Hospit
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ELAKIS George
South Eastern Area Laboratory Service, Molecular and Cytogenetics laboratory, Prince of Wales Hospit
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SMITHERS Lisa
Child Health Research Institute
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POWELL Barry
Child Health Research Institute
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Cox Timothy
Australian Craniofacial Institute Associated With The University Of Adelaide
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Elakis George
South Eastern Area Laboratory Service Molecular And Cytogenetics Laboratory Prince Of Wales Hospital
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Roscioli Tony
South Eastern Area Laboratory Service Molecular And Cytogenetics Laboratory Prince Of Wales Hospital
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DAVID David
Australian Craniofacial Unit, Women's and Children's Hospital
関連論文
- Differential Effects of FGFR2 Mutation in Ophthalmic Findings in Apert Syndrome
- Oblique Facial Clefting Associated with Unicoronal Synostosis
- Somatic FGFR and TWIST Mutations are not a Common Cause of Isolated Nonsyndromic Single Suture Craniosynostosis
- Identification of a novel FcγRIII receptor that is up-regulated in fetal wound healing