A novel MLH1 mutation in a Japanese family with Lynch syndrome associated with small bowel cancer

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 2054-345X

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: A novel MLH1 mutation in a Japanese family with Lynch syndrome associated with small bowel cancer ; volume:5 ; number:1 ; day:21 ; month:6 ; year:2018 ; pages:1-3 ; date:12.2018
Human genome variation ; 5, Heft 1 (21.6.2018), 1-3, 12.2018

Creator: Akizawa, Yoshika

Contributor: Yamamoto, Toshiyuki
Tamura, Kazuo
Kanno, Toshiyuki
Takahashi, Nobuko
Ohki, Takeshi
Omori, Teppei
Tokushige, Katsutoshi
Yamamoto, Masakazu
Saito, Kayoko
SpringerLink (Online service)

DOI: 10.1038/s41439-018-0013-y

URN: urn:nbn:de:101:1-2018083120345917334834

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:23 AM CEST

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Associated

Akizawa, Yoshika
Yamamoto, Toshiyuki
Tamura, Kazuo
Kanno, Toshiyuki
Takahashi, Nobuko
Ohki, Takeshi
Omori, Teppei
Tokushige, Katsutoshi
Yamamoto, Masakazu
Saito, Kayoko
SpringerLink (Online service)

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A novel MLH1 mutation in a Japanese family with Lynch syndrome associated with small bowel cancer

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Other Objects (12)

A novel MLH1 intronic variant in a young Japanese patient with Lynch syndrome

Novel MLH1 nonsense variant in a patient with suspected Lynch syndrome

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A rare large duplication of MLH1 identified in Lynch syndrome

A Chinese family affected by lynch syndrome caused by MLH1 mutation

MLH1 germline mutation associated with Lynch syndrome in a family followed for more than 45 years

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A novel MLH1 intronic variant in a young Japanese patient with Lynch syndrome

Novel MLH1 nonsense variant in a patient with suspected Lynch syndrome

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A rare large duplication of MLH1 identified in Lynch syndrome

A Chinese family affected by lynch syndrome caused by MLH1 mutation

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Colorectal cancer risk in patients with inflammatory bowel disease and Lynch syndrome

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A novel MLH1 intronic variant in a young Japanese patient with Lynch syndrome

Novel MLH1 nonsense variant in a patient with suspected Lynch syndrome

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