Salviati Leonardo | Clinical Genetics Unit And Hematology-oncology Laboratory Department Of Pediatrics University Of Padova
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概要
- Salviati Leonardoの詳細を見る
- 同名の論文著者
- Clinical Genetics Unit And Hematology-oncology Laboratory Department Of Pediatrics University Of Padovaの論文著者
関連著者
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TREVISSON Eva
Clinical Genetics Unit, Department of Pediatrics, University of Padova
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Salviati Leonardo
Clinical Genetics Unit And Hematology-oncology Laboratory Department Of Pediatrics University Of Padova
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Trevisson Eva
Clinical Genetics Unit and Hematology-Oncology Laboratory, Department of Pediatrics, University of Padova
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Pertegato Vanessa
Clinical Genetics Unit Department Of Pediatrics University Of Padova
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FORZAN Monica
Clinical Genetics Unit, Department of Pediatrics, University of Padova
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SALVIATI Leonardo
Clinical Genetics Unit, Department of Pediatrics, University of Padova
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CASARIN Alberto
Clinical Genetics Unit, Department of Pediatrics, University of Padova
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BRUSON Alice
Clinical Genetics Unit, Department of Pediatrics, University of Padova
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DI GIANANTONIO
Clinical Genetics Unit, Department of Pediatrics, University of Padova
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CLEMENTI Maurizio
Clinical Genetics Unit, Department of Pediatrics, University of Padova
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Bruson Alice
Clinical Genetics Unit Department Of Pediatrics University Of Padova
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Forzan Monica
Clinical Genetics Unit Department Of Pediatrics University Of Padova
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Di Gianantonio
Clinical Genetics Unit Department Of Pediatrics University Of Padova
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Casarin Alberto
Clinical Genetics Unit Department Of Pediatrics University Of Padova
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Salviati Leonardo
Clinical Genetics Unit Department Of Pediatrics University Of Padova
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SACCONI Sabrina
Centre de Reference des Maladies Neuromusculaires et CNRS UMR 6543, Faculte de Medicine, Universite de Nice
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Clementi Maurizio
Clinical Genetics Unit Department Of Pediatrics University Of Padova
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Sacconi Sabrina
Centre De Reference Des Maladies Neuromusculaires Et Cnrs Umr 6543 Faculte De Medicine Universite De Nice
著作論文
- Is CFTR 621+3 A>G a cystic fibrosis causing mutation?
- Mutation analysis of COX18 in 29 patients with isolated cytochrome c oxidase deficiency