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Publications by Patrick Franken

The CHEK2 1100delC Mutation Identifies Families With a Hereditary Breast and Colorectal Cancer Phenotype

American Journal of Human Genetics

English

Related publications

CHEK2 1100delC in Patients With Metachronous Cancers of the Breast and the Colorectum

Cancer Research

English

Carrier Risk Status Changes Resulting From Mutation Testing in Hereditary Non-Polyposis Colorectal Cancer and Hereditary Breast-Ovarian Cancer

Journal of Medical Genetics

English

Managing Families With a Hereditary Cancer Syndrome

Oncology Nursing Forum

English

Association Between CHEK2 H371Y Mutation and Response to Neoadjuvant Chemotherapy in Women With Breast Cancer

Cancer Research

English

CHEK2*1100delC Genotyping for Clinical Assessment of Breast Cancer Risk: Meta-Analyses of 26,000 Patient Cases and 27,000 Controls

Journal of Clinical Oncology

Cancer Research

English

BRCA1 and BRCA2 Mutations in Danish Families With Hereditary Breast and/or Ovarian Cancer

Acta Oncologica

Nuclear Medicine

English

Mutation Analysis of the ERCC4/FANCQ Gene in Hereditary Breast Cancer

Multidisciplinary

English

Comprehensive Genetic Characterization of Hereditary Breast/Ovarian Cancer Families From Slovakia

Breast Cancer Research and Treatment

Cancer Research

English

Knowledge About Hereditary Nonpolyposis Colorectal Cancer; Mutation Carriers and Physicians at Equal Levels

BMC Medical Genetics

English