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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.
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2018 (English)In: Hereditary Cancer in Clinical Practice, ISSN 1731-2302, E-ISSN 1897-4287, Vol. 16, article id 16Article in journal (Refereed) 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.

Place, publisher, year, edition, pages
BioMed Central, 2018. Vol. 16, article id 16
Keywords [en]
Extracolonic; Lynch syndrome; MMR genes; Tumour spectrum
National Category
Cancer and Oncology
Identifiers
URN: urn:nbn:se:liu:diva-152503DOI: 10.1186/s13053-018-0098-9ISI: 000448176600001PubMedID: 30386444OAI: oai:DiVA.org:liu-152503DiVA, id: diva2:1299661
Available from: 2019-03-28 Created: 2019-03-28 Last updated: 2019-05-03

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