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A Chinese family affected by lynch syndrome caused by MLH1 mutation.
Jia, Shuqin; Zhang, Meng; Sun, Yu; Yan, Hai; Zhao, Fangping; Li, Ziyu; Ji, Jiafu.
Afiliación
  • Jia S; Center for Molecular Diagnostics, Key laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking University Cancer Hospital & Institute, No.52 Fucheng Road, Haidian District, Beijing, 100142, China.
  • Zhang M; Center for Molecular Diagnostics, Key laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking University Cancer Hospital & Institute, No.52 Fucheng Road, Haidian District, Beijing, 100142, China.
  • Sun Y; Department of Pathology, Key laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking University Cancer Hospital & Institute, Beijing, China.
  • Yan H; Center for Molecular Diagnostics, Key laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking University Cancer Hospital & Institute, No.52 Fucheng Road, Haidian District, Beijing, 100142, China.
  • Zhao F; Department of Pathology, Duke University Medical Center, Durham, NC, USA.
  • Li Z; Genetron Health Co., Ltd, Beijing, China.
  • Ji J; Department of Gastrointestinal Surgery, Key laboratory of Carcinogenesis and Translational Research (Ministry of Education), Peking University Cancer Hospital & Institute, No.52 Fucheng Road, Haidian District, Beijing, 100142, China. ligregory369@hotmail.com.
BMC Med Genet ; 19(1): 106, 2018 06 22.
Article en En | MEDLINE | ID: mdl-29929473
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Colorrectales Hereditarias sin Poliposis / Mutación de Línea Germinal / Predisposición Genética a la Enfermedad / Pueblo Asiatico / Homólogo 1 de la Proteína MutL Tipo de estudio: Guideline / Prognostic_studies Límite: Female / Humans / Male / Middle aged Idioma: En Revista: BMC Med Genet Asunto de la revista: GENETICA MEDICA Año: 2018 Tipo del documento: Article País de afiliación: China
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Colorrectales Hereditarias sin Poliposis / Mutación de Línea Germinal / Predisposición Genética a la Enfermedad / Pueblo Asiatico / Homólogo 1 de la Proteína MutL Tipo de estudio: Guideline / Prognostic_studies Límite: Female / Humans / Male / Middle aged Idioma: En Revista: BMC Med Genet Asunto de la revista: GENETICA MEDICA Año: 2018 Tipo del documento: Article País de afiliación: China