Double heterozygosity for BRCA1 and hMLH1 gene mutations in a 46-year-old woman with five primary tumors

Germline truncating-mutations in BRCA1 and MSH6 in a patient with early onset endometrial cancer

(2012) Karin Kast et al.   BMC CANCER

Colorectal and Other Cancer Risks for Carriers and Noncarriers From Families With a DNA Mismatch Repair Gene Mutation: A Prospective Cohort Study

(2012) Aung Ko Win et al.   JOURNAL OF CLINICAL ONCOLOGY

Evidence for breast cancer as an integral part of lynch syndrome

(2011) Nicole Buerki et al.   GENES CHROMOSOMES & CANCER

Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer

(2011) Shiyu Zhang et al.   GYNECOLOGIC ONCOLOGY

Cancer Risks Associated With Germline Mutations in MLH1, MSH2, and MSH6 Genes in Lynch Syndrome

(2011) Valérie Bonadona   JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION

Mismatch repair defective breast cancer in the hereditary nonpolyposis colorectal cancer syndrome

(2009) Uffe Birk Jensen et al.   BREAST CANCER RESEARCH AND TREATMENT

Colorectal cancer in HNPCC: cumulative lifetime incidence, survival and tumour distribution. A report of 121 families with proven mutations

(2009) E Barrow et al.   CLINICAL GENETICS

Cumulative lifetime incidence of extracolonic cancers in Lynch syndrome: a report of 121 families with proven mutations

(2009) E Barrow et al.   CLINICAL GENETICS

Review of the Lynch syndrome: history, molecular genetics, screening, differential diagnosis, and medicolegal ramifications

(2009) HT Lynch et al.   CLINICAL GENETICS

Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1

(2008) Marjolijn J L Ligtenberg et al.   NATURE GENETICS