Clinical and genetic evaluation of thirty ovarian cancer families
- 1 January 1998
- journal article
- research article
- Published by Elsevier in American Journal of Obstetrics and Gynecology
- Vol. 178 (1) , 85-90
- https://doi.org/10.1016/s0002-9378(98)70632-5
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- BRCA1Mutations in Women Attending Clinics That Evaluate the Risk of Breast CancerNew England Journal of Medicine, 1997
- Mutation analysis of the BRCA2 gene in 49 site–specific breast cancer familiesNature Genetics, 1996
- Ovarian cancer risk in BRCA1 carriers is modified by the HRAS1 variable number of tandem repeat (VNTR) locusNature Genetics, 1996
- Risk modifiers in carriers of brca1 mutationsInternational Journal of Cancer, 1995
- Identification of the breast cancer susceptibility gene BRCA2Nature, 1995
- What Does It Mean to Be a Cancer Gene Carrier? Problems in Establishing Causality From the Molecular Genetics of CancerJNCI Journal of the National Cancer Institute, 1995
- Rapid detection of BRCA1 mutations by the protein truncation testNature Genetics, 1995
- Unusual case of Smith‐Lemli‐Opitz syndrome “type II”American Journal of Medical Genetics, 1995
- Hereditary Ovarian CancerInternational Journal of Gynecological Pathology, 1992
- Analysis of 138 consecutive ovarian cancer patients: Incidence and characteristics of familial casesGynecologic Oncology, 1990