Chromosomal analysis and BRCA2*617delT/88delTG and BRIP1 (c.2392C>T) mutations of Fanconi anemia in Iranian family, and its correlation to breast cancer susceptibility

Abstract

Fanconi anemia (FA) is a rare disease, but it is the most common among the inherited bone marrow failure syndromes. In the present study, one family diagnosed with Fanconi anemia was examined. There was a 22-year-old female in this family who was diagnosed with both breast cancer and with Fanconi anemia. The chromosomal breakage in karyotyping was… (More)

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Cite this paper

@inproceedings{Kooshyar2015ChromosomalAA, title={Chromosomal analysis and BRCA2*617delT/88delTG and BRIP1 (c.2392C>T) mutations of Fanconi anemia in Iranian family, and its correlation to breast cancer susceptibility}, author={Mohammad Mahdi Kooshyar and Mohammadreza Nassiri and Ehsan Ghayoor Karimiani and Mohammad Reza Doosti and Khadijeh Nasiri and Zahra Rodbari}, year={2015} }