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Toward a better definition of EPCAM deletions in Lynch Syndrome: Report of new variants in Italy and the associated molecular phenotype.
Cini, Giulia; Quaia, Michele; Canzonieri, Vincenzo; Fornasarig, Mara; Maestro, Roberta; Morabito, Alberto; D'Elia, Angela Valentina; Urso, Emanuele Damiano; Mammi, Isabella; Viel, Alessandra.
Afiliación
  • Cini G; Functional Oncogenomics and Genetics, Centro di Riferimento Oncologico di Aviano (CRO), IRCCS, Aviano, PN, Italy.
  • Quaia M; Functional Oncogenomics and Genetics, Centro di Riferimento Oncologico di Aviano (CRO), IRCCS, Aviano, PN, Italy.
  • Canzonieri V; Pathology, Centro di Riferimento Oncologico di Aviano (CRO), IRCCS, Aviano, PN, Italy.
  • Fornasarig M; Gastroenterology, Centro di Riferimento Oncologico di Aviano (CRO), IRCCS, Aviano, PN, Italy.
  • Maestro R; Functional Oncogenomics and Genetics, Centro di Riferimento Oncologico di Aviano (CRO), IRCCS, Aviano, PN, Italy.
  • Morabito A; Oncology, Cittadella, PD, Italy.
  • D'Elia AV; Department of Medical Area, University of Udine, Udine, Italy.
  • Urso ED; Department of Surgical Oncology and Gastroenterology, University of Padua, Padova, Italy.
  • Mammi I; Medical Genetics, Dolo Hospital, Dolo, VE, Italy.
  • Viel A; Functional Oncogenomics and Genetics, Centro di Riferimento Oncologico di Aviano (CRO), IRCCS, Aviano, PN, Italy.
Mol Genet Genomic Med ; 7(5): e587, 2019 05.
Article en En | MEDLINE | ID: mdl-30916491
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Colorrectales Hereditarias sin Poliposis / Eliminación de Gen / Molécula de Adhesión Celular Epitelial / Frecuencia de los Genes Tipo de estudio: Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Mol Genet Genomic Med Año: 2019 Tipo del documento: Article País de afiliación: Italia
Texto completo
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PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Colorrectales Hereditarias sin Poliposis / Eliminación de Gen / Molécula de Adhesión Celular Epitelial / Frecuencia de los Genes Tipo de estudio: Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Mol Genet Genomic Med Año: 2019 Tipo del documento: Article País de afiliación: Italia