Associated Papers
Thyroid cancers of follicular origin in a genomic light: in-depth overview of common and unique molecular marker candidates.
Pstrąg N et al.
Molecular Cancer, 2018
The Prevalence of Founder Mutations among Individuals from Families with Familial Pancreatic Cancer Syndrome.
Lener MR et al.
Cancer Research and Treatment, 2017
A risk of breast cancer in women - carriers of constitutional CHEK2 gene mutations, originating from the North - Central Poland.
Bąk A et al.
Hereditary Cancer in Clinical Practice, 2014
Identification of a novel BRCA2 and CHEK2 A-C-G-C haplotype in Turkish patients affected with breast cancer.
Haytural H et al.
Asian Pacific Journal of Cancer Prevention : Apjcp, 2013
Irrelevance of CHEK2 variants to diagnosis of breast/ovarian cancer predisposition in Polish cohort.
Myszka A et al.
Journal of Applied Genetics, 2011
CHEK2 mutations and HNPCC-related colorectal cancer.
Suchy J et al.
International Journal of Cancer, 2010
Select a paper to view details