Genetic Diagnosis of Sex and Trisomies 13, 18, 21 in Human Single Cell Embryo by Multiplex Fluorescent Polymerase Chain Reaction
Keywords:
aneuploidy, multiplex fluorescent PCR, PGDAbstract
A multiplex fluorescent PCR was developed for preimplantation genetic diagnosis (PGD) to investigate aneuploidy screening of chromosomes 13, 18, 21, X and Y in a single human blastomere. The multiplex fluorescent PCR was able to give successful amplification in 30 cases. This technique was
found to be sufficiently sensitive to reveal the peaks of trisomic alleles in 20 pg DNA of control samples. Multiplex fluorescent PCR products of short tandem repeats (STRs) located on chromosomes 13, 18, 21, X and Y from a single human blastomere in a single tube have recently been used for the detection of common chromosome aneuploidies in a single human blastomere.
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online 2452-316X print 2468-1458/Copyright © 2022. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/),
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