High frequency of BRCA1 founder mutations in Polish women with nonfamilial breast cancer

A state-wide population-based program for detection of lynch syndrome based upon immunohistochemical and molecular testing of colorectal tumours

(2011) Lyn Schofield et al.   Familial Cancer

Prevalence of the most frequent BRCA1 mutations in Polish population

(2011) Izabela Brozek et al.   JOURNAL OF APPLIED GENETICS

Novel germline mutations in BRCA2 gene among breast and breast-ovarian cancer families from Poland

(2010) Aneta Balabas et al.   Familial Cancer

The role of BRCA mutation testing in determining breast cancer therapy

(2010) Alison H. Trainer et al.   Nature Reviews Clinical Oncology

Integrating genomics, proteomics and bioinformatics in translational studies of molecular medicine

(2009) Jerzy Ostrowski et al.   EXPERT REVIEW OF MOLECULAR DIAGNOSTICS

Age at Onset of Bilateral Breast Cancer, the Presence of Hereditary BRCA1, BRCA2, CHEK2 Gene Mutations and Positive Family History of Cancer

(2009) Elżbieta Skasko et al.   Oncology Research and Treatment

Inherited Susceptibility to Common Cancers

(2008) William D. Foulkes   NEW ENGLAND JOURNAL OF MEDICINE