MONROS Eugenia | Genetics Section, Hospital Sant Joan de Deu
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概要
関連著者
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MONROS Eugenia
Genetics Section, Hospital Sant Joan de Deu
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Poo Pilar
Neurology Section Hospital Sant Joan De Deu
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Monros Eugenia
Genetics Section Hospital Sant Joan De Deu
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OKAMOTO Nobuhiko
Department of Planning and Research, Osaka Medical Center and Research Institute for Maternal and Ch
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Yamasaki Mami
Institute for Clinical Research, Osaka National Hospital, National Hospital Organization
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Kanemura Yonehiro
Tissue Engineering Research Center National Institute Of Advanced Industrial Science And Technology
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Kanemura Yonehiro
Tissue Engineering Research Center (terc) National Institute Of Advanced Industrial Science And Tech
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Yamasaki Mami
Institute For Clinical Research
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Yamasaki Mami
Institute For Clinical Research Osaka National Hospital
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DEL MAESTRO
Brain Tumor Research Center, Montreal Neurological Institute and Hospital
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VALERO Rebeca
Genetics Section, Hospital Sant Joan de Deu
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POO Pilar
Neurology Section, Hospital Sant Joan de Deu
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Poo Pilar
Neurology Service Hospital Sant Joan De Deu
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Del Maestro
Brain Tumor Research Center Montreal Neurological Institute And Hospital
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Valero Rebeca
Genetics Section Hospital Sant Joan De Deu
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Okamoto Nobuhiko
Department Of Planning And Research Osaka Medical Center And Research Institute For Maternal And Chi
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Pineda Merce
Neurology Service Hospital Sant Joan De Deu
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ARMSTRONG Judith
Genetics Section, Hospital Sant Joan de Deu
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AIBAR Elena
Genetics Section, Hospital Sant Joan de Deu
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CANOS Ignacio
Biochemistry Service, Hospital Dr. Pesset
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Aibar Elena
Genetics Section Hospital Sant Joan De Deu
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Canos Ignacio
Biochemistry Service Hospital Dr. Pesset
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Armstrong Judith
Genetics Section Hospital Sant Joan De Deu
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Okamoto Nobuhiko
Department Of Molecular Cytogenetics Medical Research Institute And School Of Biomedical Science Tokyo Medical And Dental University
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OKAMOTO Nobuhiko
Department of Medical Genetics, Osaka Medical Center and Research Institute for Maternal and Child Health
著作論文
- Hydrocephalus and Hirschsprung's disease with a mutation of L1CAM
- Rett syndrome in Spain : mutation analysis and clinical correlations