Cao Henian | Robarts Research Institute

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概要

• Cao Henianの詳細を見る
• 同名の論文著者
• Robarts Research Instituteの論文著者

関連著者

• CAO Henian

  Robarts Research Institute, University of Western Ontario

• Cao Henian

  Robarts Research Institute

• Hegele Robert

  Robarts Research Institute

• HEGELE Robert

  Blackburn Cardiovascular Genetics Laboratory, John P. Robarts Research Institute

• Kim Chong

  Genetic Unit Department Of Pediatrics University Of Sao Paulo Medical School

• Hegele Robert

  Blackburn Cardiovascular Genetics Laboratory John P. Robarts Research Institute

• Hegele Robert

  Blackburn Cardiovascular Genetics Laboratory Robarts Research Institute

• Cao Henian

  Robarts Research Institute University Of Western Ontario

• BERTOLA Debora

  Genetics Clinic Unit, Instituto da Crianca do Hospital das Clinicas, University of Sao Paulo

• ALBANO Lilian

  Genetics Clinic Unit, Instituto da Crianca do Hospital das Clinicas, University of Sao Paulo

• OLIVEIRA Daniela

  Department of Neurology, University of Sao Paulo

• KOK Fernando

  Department of Neurology, University of Sao Paulo

• MARQUES-DIAS Maria

  Department of Neurology, University of Sao Paulo

• WILLIAMS Christina

  Robarts Research Institute

• CARTER Monica

  Robarts Research Institute

• Marques-dias Maria

  Department Of Neurology University Of Sao Paulo

• Albano Lilian

  Genetics Clinic Unit Instituto Da Crianca Do Hospital Das Clinicas University Of Sao Paulo

• Bertola Debora

  Genetics Clinic Unit Instituto Da Crianca Do Hospital Das Clinicas University Of Sao Paulo

• Kok Fernando

  Department Of Neurology University Of Sao Paulo

• Kok Fernando

  Departamento De Neurologia Do Hospital Das Clinicas Da Faculdade De Medicina Da Universidade De Sao

• Oliveira Daniela

  Department Of Neurology University Of Sao Paulo

• Kim Chong

  Genetics Clinic Unit Instituto Da Crianca Do Hospital Das Clinicas University Of Sao Paulo

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著作論文

• Identification of single-nucleotide polymorphisms in the human LPIN1 gene
• Cockayne syndrome type A : novel mutations in eight typical patients
• CKN1 (MIM 216400) : mutations in Cockayne syndrome type A and a new common polymorphism

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