Differential Effects of FGFR2 Mutation in Ophthalmic Findings in Apert Syndrome
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概要
- 論文の詳細を見る
- 2007-01-01
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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Selva Dinesh
Oculoplastic And Orbital Division Department Of Ophthalmology And Visual Science University Of Adela
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KHONG Jwu
Oculoplastic and Orbital Division, Department of Ophthalmology and Visual Science, University of Ade
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HAMMERTON Michael
Australian Craniofacial Unit, Women's and Children's Hospital
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ROSCIOLI Tony
Department of Haemotology and Genetics, Prince of Wales Hospital
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Khong Jwu
Oculoplastic And Orbital Division Department Of Ophthalmology And Visual Science University Of Adela
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Roscioli Tony
South Eastern Area Laboratory Service Molecular And Cytogenetics Laboratory Prince Of Wales Hospital
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Hammerton Michael
Australian Craniofacial Unit Women's And Children's 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
- Glomus Tumour of the Eyelid