Detection of allelic imbalance in MLH1 expression by pyrosequencing serves as a tool for the identification of germline defects in Lynch syndrome

By Kwok Chau-To   Ward Robyn   Hawkins Nicholas   Hitchins Megan  

Familial Cancer, Vol. 9, Iss. 3, 2010-09 ,pp. : 345-356

Springer Publishing Company

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Relationship of lower uterine segment cancer with Lynch syndrome: A novel case with an hMLH1 germline mutation

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Oncology Reports, Vol. 28, Iss. 5, 2012-11 ,pp. : 1537-1543

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Nine novel pathogenic germline mutations in MLH1, MSH2, MSH6 and PMS2 in families with Lynch syndrome

By Rahner Nils   Friedrichs Nicolaus   Wehner Maria   Steinke Verena   Aretz Stefan   Friedl Waltraut   Buettner Reinhard   Mangold Elisabeth   Propping Peter   Walldorf Constanze  

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Correlation of MLH1 and MGMT methylation levels between peripheral blood leukocytes and colorectal tissue DNA samples in colorectal cancer patients

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Oncology Letters, Vol. 6, Iss. 5, 2013-01 ,pp. : 1370-1376

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MLH1 and MSH2 Mutations in Colombian Families with Hereditary Nonpolyposis Colorectal Cancer (Lynch syndrome) – Description of Four Novel Mutations

By Giraldo Alejandro   Gómez Andrea   Salguero Gustavo   García Herbert   Aristizábal Fabio   Gutiérrez Óscar   Ángel Luis   Padrón Jorge   Martínez Carlos   Martínez Humberto   Malaver Omar   Flórez Luis   Barvo Rosa  

Familial Cancer, Vol. 4, Iss. 4, 2005-11 ,pp. : 285-290

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