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A retrospective study of extracolonic, non-endometrial cancer in Swedish Lynch syndrome families
Department of Oncology, Karolinska University Hospital, Stockholm, Sweden.
Department of Clinical Genetics, Karolinska University Hospital, Solna, 171 76 Stockholm, Sweden; 3Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Department of Clinical Genetics, Akademiska University Hospital, Uppsala, Sweden.
Department of Clinical Genetics, Norrlands University Hospital, Umeå, Sweden.
Vise andre og tillknytning
2018 (engelsk)Inngår i: Hereditary Cancer in Clinical Practice, ISSN 1731-2302, E-ISSN 1897-4287, Vol. 16, artikkel-id 16Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Lynch Syndrome is an autosomal dominant cancer syndrome caused by pathogenic germ-line variants in one of the DNA-mismatch-repair (MMR) genes MLH1, MSH2, MSH6 or PMS2. Carriers are predisposed to colorectal and endometrial cancer, but also other cancer types. The purpose of this retrospective study was to characterize the tumour spectrum of the Swedish Lynch syndrome families.

sted, utgiver, år, opplag, sider
BioMed Central, 2018. Vol. 16, artikkel-id 16
Emneord [en]
Extracolonic; Lynch syndrome; MMR genes; Tumour spectrum
HSV kategori
Identifikatorer
URN: urn:nbn:se:liu:diva-152503DOI: 10.1186/s13053-018-0098-9ISI: 000448176600001PubMedID: 30386444OAI: oai:DiVA.org:liu-152503DiVA, id: diva2:1299661
Tilgjengelig fra: 2019-03-28 Laget: 2019-03-28 Sist oppdatert: 2019-05-03

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