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The Journal of Maternal-Fetal & Neonatal Medicine Volume 29, 2016 - Issue 16
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Original Article

Detection of paternally inherited fetal point mutations for β-thalassemia in maternal plasma using simple fetal DNA enrichment protocol with or without whole genome amplification: an accuracy assessment

Mahboubeh RamezanzadehDepartment of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran and
,
Mansour SalehiDepartment of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran and
,
Ziba FarajzadeganDepartment of Community Medicine, Isfahan University of Medical Sciences, Isfahan, Iran
,
Sara KamaliDepartment of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran and
&
Rasoul SalehiDepartment of Genetics and Molecular Biology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran and Correspondence[email protected]
Pages 2645-2649 | Received 20 Jul 2015, Accepted 15 Sep 2015, Published online: 09 Nov 2015

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Muhammad Afzal, Muhammad Abdul Naeem, Suhaib Ahmed, Nayyar Amin, Amena Rahim, Manazza Munawar, Mansoor Ishaq, Ali Rathore & K. Maria. (2022) Noninvasive prenatal testing of beta-thalassemia for common Pakistani mutations: a comparative study using cell-free fetal DNA from maternal plasma and chorionic villus sampling. Hematology 27:1, pages 353-359.
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Articles from other publishers (2)

Yu Tan, Hui Jian, Ranran Zhang, Jing Wang, Cong Zhou, Yuanyuan Xiao, Weibo Liang & Li Wang. (2023) Applying amplification refractory mutation system technique to detecting cell-free fetal DNA for single-gene disorders purpose. Frontiers in Genetics 14.
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Mahboubeh Ramezanzadeh, Sharifeh Khosravi & Rasoul Salehi. (2017) Cell-free Fetal Nucleic Acid Identifier Markers in Maternal Circulation. Advanced Biomedical Research 6:1, pages 89.
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