Germline PTEN mutations are rare and highly penetrant
Open Access
- 1 January 2006
- journal article
- Published by Springer Science and Business Media LLC in Hereditary Cancer in Clinical Practice
- Vol. 4 (4), 177-85
- https://doi.org/10.1186/1897-4287-4-4-177
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Genetic conditions associated with intestinal juvenile polypsAmerican Journal Of Medical Genetics Part C-Seminars In Medical Genetics, 2004
- Hereditary Colorectal CancerNew England Journal of Medicine, 2003
- PTEN Mutation Spectrum and Genotype-Phenotype Correlations in Bannayan-Riley-Ruvalcaba Syndrome Suggest a Single Entity With Cowden SyndromeHuman Molecular Genetics, 1999
- Novel PTEN mutations in patients with Cowden disease: absence of clear genotype–phenotype correlationsEuropean Journal of Human Genetics, 1999
- Germline mutations in PTEN are an infrequent cause of genetic predisposition to breast cancerOncogene, 1998
- Genetics of Cowden syndrome: through the looking glass of oncology.International Journal of Oncology, 1998
- Inherited Mutations in PTEN That Are Associated with Breast Cancer, Cowden Disease, and Juvenile PolyposisAmerican Journal of Human Genetics, 1997
- Germline mutations in the PTEN/MMAC1 gene in patients with Cowden diseaseHuman Molecular Genetics, 1997
- Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndromeNature Genetics, 1997
- The Cowden syndrome: a clinical and genetic study in 21 patientsClinical Genetics, 1986