Cargando…
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...
Autores principales: | Miresmaeili, Seyed Mohsen, Kordi Tamandani, Dor Mohammad, Kalantar, Seyed Mehdi, Moshtaghioun, Seyed Mohammad |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Research and Clinical Center for Infertility
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4918776/ https://www.ncbi.nlm.nih.gov/pubmed/27351029 |
Ejemplares similares
-
A Novel Mutation-BRCA1 Associated Hereditary Haplotype of Intragenic Markers of BRCA1 Gene in a Family with History of Breast Cancer
por: Miresmaeili, Seyed Mohsen, et al.
Publicado: (2019) -
BRCA1 and BRCA2 mutations in Iranian breast cancer patients: A systematic review
por: Neamatzadeh, Hossein, et al.
Publicado: (2015) -
Strategies for whole-exome sequencing analysis in a case series study of familial male infertility
por: Askari, Masomeh, et al.
Publicado: (2020) -
Novel Mutations of the CHRNA3 Gene in Non-Small Cell Lung Cancer in an Iranian Population
por: Mehrabi, Nahid, et al.
Publicado: (2017) -
Identification of a TPP1 Q278X Mutation in an Iranian Patient with Neuronal Ceroid Lipofuscinosis 2: Literature Review and Mutations Update
por: Baranzehi, Tayebeh, et al.
Publicado: (2022)