Screening of the DNA mismatch repair genes MLH1, MSH2 and MSH6in a Greek cohort of Lynch syndrome suspected families
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1471-2407
- Extent
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Online-Ressource
- Language
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Englisch
- Notes
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online resource.
- Bibliographic citation
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Screening of the DNA mismatch repair genes MLH1, MSH2 and MSH6in a Greek cohort of Lynch syndrome suspected families ; volume:10 ; number:1 ; day:11 ; month:10 ; year:2010 ; pages:1-12 ; date:12.2010
BMC cancer ; 10, Heft 1 (11.10.2010), 1-12, 12.2010
- Creator
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Thodi, Georgia
- Contributor
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Fostira, Florentia
Sandaltzopoulos, Raphael
Nasioulas, George
Grivas, Anastasios
Boukovinas, Ioannis
Mylonaki, Maria
Panopoulos, Christos
Magic, Mirjana Brankovic
Fountzilas, George
Yannoukakos, Drakoulis
SpringerLink (Online service)
- DOI
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10.1186/1471-2407-10-544
- URN
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urn:nbn:de:1111-2016030355469
- Rights
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Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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15.08.2025, 7:37 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Thodi, Georgia
- Fostira, Florentia
- Sandaltzopoulos, Raphael
- Nasioulas, George
- Grivas, Anastasios
- Boukovinas, Ioannis
- Mylonaki, Maria
- Panopoulos, Christos
- Magic, Mirjana Brankovic
- Fountzilas, George
- Yannoukakos, Drakoulis
- SpringerLink (Online service)
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Analyse von im Lynch-Syndrom identifizierten MLH1-Keimbahnmutationen auf molekulare und zelluläre Aspekte der DNA-Mismatch-Reparatur
Analyse von im Lynch-Syndrom identifizierten MLH1-Keimbahnmutationen auf molekulare und zelluläre Aspekte der DNA Mismatch-Reparatur
Funktionelle Analyse des MLH1·ITGA9-Fusionsproteins einer Lynch-Syndrom-Familie
A rare large duplication of MLH1 identified in Lynch syndrome
Identification of new genetic alterations in MLH1, MSH2 and MSH6 using IHC and HRM analysis in Lynch syndrome-suspected patients
A Chinese family affected by lynch syndrome caused by MLH1 mutation
Lynch syndrome-associated endometrial carcinoma with MLH1 germline mutation and MLH1 promoter hypermethylation: a case report and literature review
MLH1 Exon 12 Gene Deletion Leading to Lynch Syndrome: A Case Report
A tumor focused approach to resolving the etiology of DNA mismatch repair deficient tumors classified as suspected Lynch syndrome
A novel MLH1 intronic variant in a young Japanese patient with Lynch syndrome