Endometrial tumour BRAF mutations and MLH1 promoter methylation as predictors of germline mismatch repair gene mutation status: a literature review

By Metcalf Alexander   Spurdle Amanda  

Familial Cancer, Vol. 13, Iss. 1, 2014-03 ,pp. : 1-12

Springer Publishing Company

Access to resources Recommend Favorite

Screening for exonic copy number mutations at MSH2 and MLH1 by MAPH

By Akrami Seyed   Dunlop Malcolm   Farrington Susan   Frayling Ian   MacDonald Fiona   Harvey John   Armour John  

Familial Cancer, Vol. 4, Iss. 2, 2005-06 ,pp. : 145-149

Springer Publishing Company

Access to resources Recommend Favorite

No association of (−131C→G) variant of CHI3L1 gene with risk of glioblastoma and prognosis

By Boisselier Blandine   Marie Yannick   El Hallani Soufiane   Kaloshi Gentian   Iershov Anton   Kavsan Vadym   Psimaras Dimitri   Thillet Joëlle   Hoang-Xuan Khe   Delattre Jean-Yves   Sanson Marc  

Journal of Neuro-Oncology, Vol. 94, Iss. 2, 2009-09 ,pp. : 169-172

Springer Publishing Company

Access to resources Recommend Favorite

Lynch syndrome: the influence of environmental factors on extracolonic cancer risk in hMLH1 c.C1528T mutation carriers and their mutation-negative sisters

By Blokhuis M.   Pietersen G.   Goldberg P.   Algar U.   Merwe L.   Mbatani N.   Vorster A.   Ramesar R.  

Familial Cancer, Vol. 9, Iss. 3, 2010-09 ,pp. : 357-363

Springer Publishing Company

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite