FGFR2 mutation and genotype-phenotype analysis in eight Japanese patients associated with Apert syndrome
スポンサーリンク
概要
著者
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SUZUKI Hideaki
Institute for Solid State Physics, The University of Tokyo
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Eto Yoshikatsu
Institute Of Dna Medicine Jikei University School Of Medicine:department Of Pediatrics Jikei Univers
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TSUKUNO Mari
Department of Applied Chemistry, Tokai University
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Ninomiya Kunitoshi
Department of Plastic and Reconstructive Surgery, Jikei University School of Medicine
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Kurihara Kunihiro
Department of Plastic and Reconstructive Surgery, Jikei University School of Medicine
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Kurihara Kunihiro
Department Of Plastic And Reconstructive Surgery Jikei University School Of Medicine
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Kurihara Kunihiro
Department Of Plastic And Reconstructive Surgery
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Ninomiya K
Department Of Plastic And Reconstructive Surgery Jikei University School Of Medicine
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Tsukuno Mari
Department Of Plastic And Reconstructive Surgery Jikei University School Of Medicine:institute Of Dn
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Tsukuno Mari
Department Of Applied Chemistry Tokai University
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Suzuki Hideaki
Institute Of Dna Medicine Jikei University School Of Medicine:department Of Pediatrics Jikei Univers
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Suzuki Hideaki
Institute For Solid State Physics University Of Tokyo
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Suzuki Hideaki
Institute For Solid State Physics The University Of Tokyo
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- FGFR2 mutation and genotype-phenotype analysis in eight Japanese patients associated with Apert syndrome
- An Atypical Case of Unilateral Lacrimal Gland Hyperplasia
- Metallic Transport and Ferrimagnetic Interaction Achieved by Band Filling Control in Organic Conductors; β'-ET_3(MCl_4^)_(M'Cl_4^)_x[M=Co, Zn, M'=Ga, Fe](Condensed Matter: Electronic Structure, Electrical, Magnetic and Optical Properties)