Last Posted: Jun-24-2019 11AM
Last Posted: Jun 24, 2019
- [III. Hereditary Breast and/or Ovarian Cancer Syndrome].
Sugitani Ikuko et al. Gan to kagaku ryoho. Cancer & chemotherapy 2018 Dec 45(12) 1720-1724 - Residual glandular tissue (RGT) in BRCA1/2 germline mutation carriers with unilateral and bilateral prophylactic mastectomies.
Grinstein Olga et al. Surgical oncology 2019 Jun 29126-133 - Analysis of hereditary cancer syndromes by using a panel of genes: novel and multiple pathogenic mutations.
Tsaousis Georgios N et al. BMC cancer 2019 Jun 19(1) 535 - Clinical characteristics and outcomes in elderly women with BRCA1 and BRCA2 mutations.
Salyer Chelsea et al. Gynecologic oncology 2019 May - Hereditary Cancer Syndromes-A Primer on Diagnosis and Management: Part 1: Breast-Ovarian Cancer Syndromes.
Samadder N Jewel et al. Mayo Clinic proceedings 2019 Jun 94(6) 1084-1098 - High-Resolution Bisulfite-Sequencing of Peripheral Blood DNA Methylation in Early-Onset and Familial Risk Breast Cancer Patients.
Chen Justin et al. Clinical cancer research : an official journal of the American Association for Cancer Research 2019 Jun - Understanding Factors Associated with Uptake of BRCA1/2 Genetic Testing among Orthodox Jewish Women in the USA Using a Mixed-Methods Approach.
Trivedi Meghna S et al. Public health genomics 2019 Jun 1-11 - Comprehensive mutation detection of BRCA1/2 genes reveals large genomic rearrangements contribute to hereditary breast and ovarian cancer in Chinese women.
Cao Wen-Ming et al. BMC cancer 2019 Jun 19(1) 551 - Genetic testing and eHealth usage among Deaf women.
Kushalnagar Poorna et al. Journal of genetic counseling 2019 Jun - Evaluation of Cancer-Based Criteria for Use in Mainstream BRCA1 and BRCA2 Genetic Testing in Patients With Breast Cancer.
Kemp Zoe et al. JAMA network open 2019 May 2(5) e194428
No hay comentarios:
Publicar un comentario