Juvenile polyposis, hereditary hemorrhagic telangiectasia, and early onset colorectal cancer in patients with SMAD4 mutation
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概要
- 論文の詳細を見る
- 2012-07-01
著者
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Cohen Zane
Zane Cohen Familial Gastro-intestinal Cancer Registry Department Of Surgery Mount Sinai Hospital
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SCHWENTER Frank
Samuel Lunenfeld Research Institute, Mount Sinai Hospital, University of Toronto
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FAUGHNAN Marie
Division of Respirology, Department of Medicine, Toronto HHT Centre, St. Michael's Hospital
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GRADINGER Abigail
Zane Cohen Familial Gastro-Intestinal Cancer Registry, Department of Surgery, Mount Sinai Hospital
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BERK Terri
Zane Cohen Familial Gastro-Intestinal Cancer Registry, Department of Surgery, Mount Sinai Hospital
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GRYFE Robert
Zane Cohen Familial Gastro-Intestinal Cancer Registry, Department of Surgery, Mount Sinai Hospital
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POLLETT Aaron
Department of Pathology and Laboratory Medicine, Mount Sinai Hospital, University of Toronto
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GALLINGER Steven
Samuel Lunenfeld Research Institute, Mount Sinai Hospital, University of Toronto
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DURNO Carol
Zane Cohen Familial Gastro-Intestinal Cancer Registry, Department of Surgery, Mount Sinai Hospital
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Berk Terri
Zane Cohen Familial Gastro-intestinal Cancer Registry Department Of Surgery Mount Sinai Hospital
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Durno Carol
Zane Cohen Familial Gastro-intestinal Cancer Registry Department Of Surgery Mount Sinai Hospital
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Faughnan Marie
Division Of Respirology Department Of Medicine Toronto Hht Centre St. Michael's Hospital
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Gallinger Steven
Samuel Lunenfeld Research Institute Mount Sinai Hospital University Of Toronto
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Gradinger Abigail
Zane Cohen Familial Gastro-intestinal Cancer Registry Department Of Surgery Mount Sinai Hospital
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Gryfe Robert
Zane Cohen Familial Gastro-intestinal Cancer Registry Department Of Surgery Mount Sinai Hospital
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Schwenter Frank
Samuel Lunenfeld Research Institute Mount Sinai Hospital University Of Toronto
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Pollett Aaron
Department Of Laboratory Medicine And Pathobiology University Of Toronto
関連論文
- Juvenile polyposis, hereditary hemorrhagic telangiectasia, and early onset colorectal cancer in patients with SMAD4 mutation
- A novel complex mutation in MSH2 contributes to both Muir-Torre and Lynch Syndrome