Ductal carcinoma in situ in a 25-year-old man presenting with apparent unilateral gynecomastia.

A candidate gene study of folate-associated one carbon metabolism genes and colorectal cancer risk.

[Familial adenomatous polyposis: a follow-up of the extracolonic manifestations]

Robust multi-tissue gene panel for cancer detection.

Effect of genome-wide association studies, direct-to-consumer genetic testing, and high-speed sequencing technologies on predictive genetic counselling for cancer risk.

Hopefulness predicts resilience after hereditary colorectal cancer genetic testing: a prospective outcome trajectories study.

Three novel mutations of the APC gene in Korean patients with familial adenomatous polyposis.

TTD consensus document on the diagnosis and management of hereditary colorectal cancer.

Impact of gene patents and licensing practices on access to genetic testing for inherited susceptibility to cancer: comparing breast and ovarian cancers with colon cancers.

Hereditary and familial colon cancer.

Genetic and familial factors influencing breast, colon, prostate and lung cancers.

The differential diagnosis and surveillance of hereditary gastrointestinal polyposis syndromes.

The contribution of founder mutations in BRCA1 to breast and ovarian cancer in Lithuania.

Spectrum of MLH1 and MSH2 mutations in Chilean families with suspected Lynch syndrome.

[Current update and testing procedures for genetic diagnosis in malignant neoplasm: additional information on pathological tests]

Lynch syndrome-associated breast cancers: clinicopathologic characteristics of a case series from the colon cancer family registry.

Could APC gene screening be useful in children with hepatoblastoma? Early onset of adenocarcinoma in a child with familial adenomatous polyposis and hepatoblastoma.

Parental attitudes, beliefs, and perceptions about genetic testing for FAP and colorectal cancer surveillance in minors.

But is the platter really silver?

Secondary Prevention of Colorectal Cancer: Is There an Optimal Follow-up for Patients with Colorectal Cancer?

Gardner syndrome: skin manifestations, differential diagnosis and management.

The Italian external quality control program for familial adenomatous polyposis of the colon: five years of experience.

Genetic inactivation of AKT1, AKT2, and PDPK1 in human colorectal cancer cells clarifies their roles in tumor growth regulation.

DNA mismatch repair deficiency in sporadic colorectal cancer and Lynch syndrome.

Hereditary cancer predisposition syndromes and preimplantation genetic diagnosis: where are we now?