has been cited by the following article(s):
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[1]
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An experience in prenatal diagnosis via QF-PCR of a female child with a 9.9 Mb pure deletion at 18p11. 32–11.22
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2020 |
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[2]
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PRENATAL DIAGNOSIS FOR TRISOMY 21, 18 AND 13 BY QUANTITATIVE FLUORESCENT POLYMERASE CHAIN REACTION AMONG PREGNANT WOMEN WITH HIGH RISK
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JOURNAL OF MEDICINE AND PHARMACY,
2018 |
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[3]
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Results of the use of the medical technology to determine the most frequent aneuploidies by multilocus quantitative fluorescent PCR
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2016 |
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[4]
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Результаты использования медицинской технологии определения наиболее частых анеуплоидий методом многолокусной количественной флуоресцентной …
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2016 |
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[5]
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Genetic variations of 21 STR markers on chromosomes 13, 18, 21, X, and Y in the south Iranian population.
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2016 |
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[6]
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Результаты использования медицинской технологии определения наиболее частых анеуплоидий методом многолокусной количественной флуоресцентной …
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2016 |
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[7]
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Genetic variations of 21 STR markers on chromosomes 13, 18, 21, X, and Y in the south Iranian population
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Genetics and …,
2016 |
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[8]
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When They Mutate
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2015 |
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[9]
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Comparison of the Performance of QF-PCR with QPCR as A Rapid Molecular-Based Method for Sex Chromosome Aneuploidies Detection
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2014 |
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[10]
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Intersecting ellipsoids for determining chromosome number aberrations with FISH in interphase and metaphase cells
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2014 |
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[11]
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The use of Quantitative fluorescence PCR for common Aneuploidy Detection in Prenatal Diagnosis
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2014 |
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[12]
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CHẨN ĐOÁN TRƯỚC SINH CÁC TRISOMY 21, 18 VÀ 13 BẰNG KỸ THUẬT QF-PCR Ở NHÓM THAI PHỤ CÓ NGUY CƠ CAO
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[1]
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PRENATAL DIAGNOSIS FOR TRISOMY 21, 18 AND 13 BY QUANTITATIVE FLUORESCENT POLYMERASE CHAIN REACTION AMONG PREGNANT WOMEN WITH HIGH RISK
Journal of Medicine and Pharmacy,
2018
DOI:10.34071/jmp.2018.4.13
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