Holoprosencephaly and preaxial polydactyly associated with a 1.24Mb duplication encompassing FBXW11 at 5q35.1
スポンサーリンク
概要
- 論文の詳細を見る
- Springer-Verlag Tokyoの論文
- 2006-08-01
著者
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De Vries
Department Of Behavioral Biology Utrecht University
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Stroink Hans
Department Of Neurology St. Elisabeth And Tweesteden Hospital
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Van Kessel
Department Of Human Genetics Radboud University Nijmegen Medical Centre
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Stroink Hans
Department Of Child Neurology University Hospital Dijkzigt And Sophia Children's Hospital
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KOOLEN David
Department of Human Genetics, Radboud University Nijmegen Medical Centre
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HERBERGS Jos
Department of Clinical Genetics, Academic Hospital
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VELTMAN Joris
Department of Human Genetics, Radboud University Nijmegen Medical Centre
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PFUNDT Rolph
Department of Human Genetics, Radboud University Nijmegen Medical Centre
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VAN BOKHOVEN
Department of Human Genetics, Radboud University Nijmegen Medical Centre
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SISTERMANS Eirk
Department of Human Genetics, Radboud University Nijmegen Medical Centre
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BRUNNER Han
Department of Human Genetics, Radboud University Nijmegen Medical Centre
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Brunner Han
Department Of Human Genetics Radboud University Nijmegen Medical Centre
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Koolen David
Department Of Human Genetics Radboud University Nijmegen Medical Centre
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Van Bokhoven
Department Of Human Genetics Radboud University Nijmegen Medical Centre
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Pfundt Rolph
Department Of Human Genetics Radboud University Nijmegen Medical Centre
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Herbergs Jos
Department Of Clinical Genetics Academic Hospital
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Veltman Joris
Department Of Human Genetics Radboud University Nijmegen Medical Centre
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Sistermans Eirk
Department Of Human Genetics Radboud University Nijmegen Medical Centre
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De Vries
Department Of Human Genetics Radboud University Nijmegen Medical Centre
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