Haplotype analysis of BRCA1 intragenic markers in Iranian patients with familial breast and ovarian cancer
Background: Breast cancer is the most common malignancy in women. Breast Cancer Type 1 Susceptibility gene (BRCA1) is a tumor suppressor gene, involved in DNA damage repair and in 81% of the breast-ovarian cancer families were due to BRCA1. In some clinically investigated genes, the intragenic marke...
Main Authors: | Seyed Mohsen Miresmaeili, Dor Mohammad Kordi Tamandani, Seyed Mehdi Kalantar, Seyed Mohammad Moshtaghioun |
---|---|
Format: | Article |
Language: | English |
Published: |
Shahid Sadoughi University of Medical Science, Yazd, Iran
2016-04-01
|
Series: | Iranian Journal of Reproductive Medicine |
Online Access: | http://www.ssu.ac.ir/ijrm/index.php/ijrm/article/view/1907/970 |
Similar Items
-
Detection of a novel mutations in Exon 11 of BRCA1 gene in the patients with hereditary breast cancer
by: seyed mohsen miresmaeili, et al.
Published: (2019-01-01) -
BRCA1 and BRCA2 mutations in Iranian breast cancer patients: A systematic review
by: Hossein Neamatzadeh, et al.
Published: (2015-01-01) -
Association of Metformin Pharmacogenetic with a Single Amino Acid Alteration in Peroxisome Proliferator-Activated Receptor Gamma (PPARγ) Genein Patients with Polycystic Ovary Syndrome
by: Fatemeh Jafari, et al.
Published: (2019-12-01) -
Strategies for whole-exome sequencing analysis in a case series study of familial male infertility
by: Masomeh Askari, et al.
Published: (2020-05-01) -
High occurrence of <it>BRCA1 </it>intragenic rearrangements in hereditary breast and ovarian cancer syndrome in the Czech Republic
by: Kuklova Jitka, et al.
Published: (2007-06-01)