A novel missense mutation in the EDA gene associated with X-linked recessive isolated hypodontia
スポンサーリンク
概要
- 論文の詳細を見る
- Springer Japanの論文
- 2008-10-01
著者
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Dahl Niklas
Department Of Genetics And Pathology The Rudbeck Laboratory Uppsala University And University Hospit
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Ali Amjad
Human Molecular Genetics Laboratory Health Biotechnology Division National Institute For Biotechnolo
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Tariq Muhammad
Human Molecular Genetics Laboratory Health Biotechnology Division National Institute For Biotechnolo
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RASOOL Mahmood
Human Molecular Genetics Laboratory, Health Biotechnology Division, National Institute for Biotechno
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SCHUSTER Jens
Department of Genetics and Pathology, The Rudbeck Laboratory, Uppsala University and University Hosp
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ASLAM Muhammad
Human Molecular Genetics Laboratory, Health Biotechnology Division, National Institute for Biotechno
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AHMAD Ilyas
Human Molecular Genetics Laboratory, Health Biotechnology Division, National Institute for Biotechno
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ENTESARIAN Miriam
Department of Genetics and Pathology, The Rudbeck Laboratory, Uppsala University and University Hosp
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BAIG Shahid
Human Molecular Genetics Laboratory, Health Biotechnology Division, National Institute for Biotechno
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Baig Shahid
Human Molecular Genetics Laboratory Health Biotechnology Division National Institute For Biotechnolo
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Ahmad Ilyas
Human Molecular Genetics Laboratory Health Biotechnology Division National Institute For Biotechnolo
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Schuster Jens
Department Of Genetics And Pathology The Rudbeck Laboratory Uppsala University And University Hospit
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Rasool Mahmood
Human Molecular Genetics Laboratory Health Biotechnology Division National Institute For Biotechnolo
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Aslam Muhammad
Human Molecular Genetics Laboratory Health Biotechnology Division National Institute For Biotechnolo
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Entesarian Miriam
Department Of Genetics And Pathology The Rudbeck Laboratory Uppsala University And University Hospit
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Dahl Niklas
Department Of Genetics And Pathology The Rudbeck Laboratory Uppsala University
関連論文
- A novel missense mutation in the EDA gene associated with X-linked recessive isolated hypodontia
- Familiar Meniere's disease restricted to 1.48Mb on chromosome 12p12.3 by allelic and haplotype association