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Targeted gene sequencing of Lynch syndrome-related and sporadic endometrial carcinomas.
Libera, Laura; Craparotta, Ilaria; Sahnane, Nora; Chiaravalli, Anna Maria; Mannarino, Laura; Cerutti, Roberta; Riva, Cristina; Marchini, Sergio; Furlan, Daniela.
Afiliação
  • Libera L; Unit of Pathology, Department of Medicine and Surgery, University of Insubria, 21100, Varese, Italy.
  • Craparotta I; IRCCS Institute for Pharmacological Researches Mario Negri, Department of Oncology, 20156, Milano, Italy.
  • Sahnane N; Unit of Pathology, Department of Medicine and Surgery, University of Insubria, 21100, Varese, Italy; Research Center for the study of Hereditary and Familial Tumors, Department of Medicine and Surgery, University of Insubria, 21100, Varese, Italy. Electronic address: n.sahnane@gmail.com.
  • Chiaravalli AM; Research Center for the study of Hereditary and Familial Tumors, Department of Medicine and Surgery, University of Insubria, 21100, Varese, Italy; Unit of Pathology, ASST-Sette Laghi, 21100, Varese, Italy.
  • Mannarino L; IRCCS Institute for Pharmacological Researches Mario Negri, Department of Oncology, 20156, Milano, Italy.
  • Cerutti R; Unit of Pathology, Department of Medicine and Surgery, University of Insubria, 21100, Varese, Italy; Research Center for the study of Hereditary and Familial Tumors, Department of Medicine and Surgery, University of Insubria, 21100, Varese, Italy.
  • Riva C; Unit of Pathology, Department of Medicine and Surgery, University of Insubria, 21100, Varese, Italy; Research Center for the study of Hereditary and Familial Tumors, Department of Medicine and Surgery, University of Insubria, 21100, Varese, Italy.
  • Marchini S; IRCCS Institute for Pharmacological Researches Mario Negri, Department of Oncology, 20156, Milano, Italy.
  • Furlan D; Unit of Pathology, Department of Medicine and Surgery, University of Insubria, 21100, Varese, Italy; Research Center for the study of Hereditary and Familial Tumors, Department of Medicine and Surgery, University of Insubria, 21100, Varese, Italy.
Hum Pathol ; 81: 235-244, 2018 11.
Article em En | MEDLINE | ID: mdl-30420047
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Análise Mutacional de DNA / Neoplasias Colorretais Hereditárias sem Polipose / Biomarcadores Tumorais / Neoplasias do Endométrio / Pareamento Incorreto de Bases / Perfilação da Expressão Gênica / Instabilidade de Microssatélites / Sequenciamento de Nucleotídeos em Larga Escala / Mutação Tipo de estudo: Prognostic_studies Limite: Adult / Aged / Female / Humans / Middle aged Idioma: En Revista: Hum Pathol Assunto da revista: PATOLOGIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Itália
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Análise Mutacional de DNA / Neoplasias Colorretais Hereditárias sem Polipose / Biomarcadores Tumorais / Neoplasias do Endométrio / Pareamento Incorreto de Bases / Perfilação da Expressão Gênica / Instabilidade de Microssatélites / Sequenciamento de Nucleotídeos em Larga Escala / Mutação Tipo de estudo: Prognostic_studies Limite: Adult / Aged / Female / Humans / Middle aged Idioma: En Revista: Hum Pathol Assunto da revista: PATOLOGIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Itália