Scheffer Ingrid | Department Of Medicine (neurology) Royal Children's Hospital And Monash Medical Centre Austin A
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概要
- SCHEFFER Ingrid E.の詳細を見る
- 同名の論文著者
- Department Of Medicine (neurology) Royal Children's Hospital And Monash Medical Centre Austin Aの論文著者
関連著者
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Scheffer Ingrid
Department Of Medicine (neurology) Royal Children's Hospital And Monash Medical Centre Austin A
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Scheffer Ingrid
Department Of Medicine The University Of Melbourne Austin Health
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Berkovic Samuel
Department Of Neurology University Of Melbourne Austin Hospital
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Berkovic Samuel
Department Of Medicine (neurology) The University Of Melbourne
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Berkovic Samuel
Department Of Medicine (neurology) Austin And Repatriation Medical Centre University Of Melbourne
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Berkovic Samuel
University Of Melbourne Austin And Repatriation Medical Centre
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Jansen Floor
Rudolph Magnus Institute Of Neuroscience Department Of Paediatric Neurology University Medical Cente
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Berkovic Samuel
Epilepsy Research Centre And Department Of Medicine (neurology) University Of Melbourne
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Berkovic Sam
Department Of Neurology University Of Melbourne Austin And Repatriation Medical Centre And Royal Chi
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Zhang Yue-hua
Department Of Paediatrics Peking University First Hospital
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Steinlein Ortrud
Institute Of Human Genetics University Hospital Bonn
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Steinlein Ortrud
Institute For Human Genetics Friedrich-wilhelms-university Of Bonn
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Steinlein Ortrud
Institut Fur Humangenetik Rheinische Friendrich-wilhelms-universitat
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CROSSLAND Kathryn
Epilepsy Research Institute, Department of Medicine (Neurology) The University of Melbourne
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Dibbens Leanne
Department Of Genetic Medicine Women's And Children's Hospital
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Scheffer Ingrid
University Of Melbourne Austin And Repatriation Medical Centre
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Scheffer Ingrid
Austin Hospital University Of Melbourne
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Scheffer Ingrid
Department Of Neurology University Of Melbourne Austin And Repatriation Medical Centre And Royal Chi
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Scheffer Ingrid
Department Of Medicine (neurology) University Of Melbourne Austin & Repatriation Medical Centre
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SINGH Rita
Department of Medicine (Neurology), The University of Melbourne
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GARDNER R.
Murdoch Children's Research Institute, Royal Children's Hospital
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CROSSLAND Kathryn
Department of Medicine (Neurology), The University of Melbourne
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Crossland Kathryn
Department Of Medicine (neurology) The University Of Melbourne
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Singh Rita
Department Of Medicine (neurology) The University Of Melbourne
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Scheffer Ingrid
Department Of Medicine (neurology) The University Of Melbourne
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STOODT Jens
Institute for Human Genetics, Friedrich-Wilhelms-University of Bonn
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MULEEY John
Department of Cytogenetics and Molecular Genetics, Women's and Children's Hospital and Department of
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BRODTKORB Eylert
Department of Neurology, Trondheim University Hospital
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Stoodt Jens
Institute For Human Genetics Friedrich-wilhelms-university Of Bonn
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Muleey John
Department Of Cytogenetics And Molecular Genetics Women's And Children's Hospital And Depa
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Brodtkorb Eylert
Department Of Neurology Trondheim University Hospital
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Brodtkorb Eylert
Department Of Neurology And Clinical Neurophysiology St. Olav's Hospital
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Berkovic Samuel
Department Of Medicine (neurology) University Of Melbourne Austin & Repatriation Medical Centre
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Gardner R.
Murdoch Children's Research Institute Royal Children's Hospital
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STROMME Petter
Department of Cytogenetics and Molecular Genetics, Women's and Children's Hospital
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MANGELSDORF Marie
Department of Cytogenetics and Molecular Genetics, Women's and Children's Hospital
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GECZ Jozef
Department of Cytogenetics and Molecular Genetics, Women's and Children's Hospital
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Gecz Jozef
Department Of Cytogenetics And Molecular Genetics Women's And Children's Hospital
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Stromme Petter
Department Of Cytogenetics And Molecular Genetics Women's And Children's Hospital
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Mangelsdorf Marie
Department Of Cytogenetics And Molecular Genetics Women's And Children's Hospital
著作論文
- Dravet syndrome or genetic (generalized) epilepsy with febrile seizures plus?
- Chromosomal Abnormalities and Epilepsy : A Review for Clinicians and Gene Hunters
- Epilesies with single gene inheritance
- Independent Occurrence of the CHRNA4 Ser248Phe Mutation in a Norwegian Family with Nocturnal Frontal Lobe Epilepsy
- Infantile spasms, dystonia, and other X-linked phenotypes caused by mutations in Aristaless related homeobox gene, ARX