A Novel Mutation of <i>MSH2</i> Gene in a Patient with Lynch Syndrome Presenting with Thirteen Metachronous Malignancies.

Silinskaite, Ugne; Gaveliene, Edita; Stulpinas, Rokas; Janavicius, Ramunas; Poskus, Tomas

A Novel Mutation of MSH2 Gene in a Patient with Lynch Syndrome Presenting with Thirteen Metachronous Malignancies.

Silinskaite, Ugne; Gaveliene, Edita; Stulpinas, Rokas; Janavicius, Ramunas; Poskus, Tomas.

Afiliación

Silinskaite U; Faculty of Medicine, Vilnius University, LT-03101 Vilnius, Lithuania.
Gaveliene E; Institute of Clinical Medicine, Faculty of Medicine, Vilnius University, LT-03101 Vilnius, Lithuania.
Stulpinas R; Department of Pathology, Forensic Medicine and Pharmacology, Institute of Biomedical Sciences, Faculty of Medicine, Vilnius University, LT-03101 Vilnius, Lithuania.
Janavicius R; National Center of Pathology, Vilnius University Hospital Santaros Clinics, LT-08406 Vilnius, Lithuania.
Poskus T; Department of Oncogenetics, Hematology, Oncology and Transfusion Medicine Center, Vilnius University Hospital Santaros Clinics, LT-08661 Vilnius, Lithuania.

J Clin Med ; 12(17)2023 Aug 24.

Article en En | MEDLINE | ID: mdl-37685569

Palabras clave

detection; hereditary nonpolyposis colorectal cancer; lynch syndrome; metachronous cancer; multiple malignancies; surveillance; tumor

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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: J Clin Med Año: 2023 Tipo del documento: Article País de afiliación: Lituania

Texto completo

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XML

PubMed Links

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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: J Clin Med Año: 2023 Tipo del documento: Article País de afiliación: Lituania