Rapid diagnosis of trisomy 13 of maternal origin by quantitative fluorescent polymerase chain reaction analysis in a pregnancy with fetal holoprosencephaly, premaxillary agenesis, postaxial polydactyly of left hand and overriding aorta

Objective: We present rapid diagnosis of trisomy 13 of maternal origin by quantitative fluorescent polymerase chain reaction (QF-PCR) in a pregnancy with multiple fetal abnormalities. Case report: A 35-year-old, primigravid woman was referred for amniocentesis at 24 weeks of gestation because of mul...

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Autori principali:	Chih-Ping Chen, Chao-Yun Wu, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Mang-Shang Lee, Wayseen Wang
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	Elsevier 2021-09-01
Serie:	Taiwanese Journal of Obstetrics & Gynecology
Soggetti:	Congenital heart defect Holoprosencephaly Polydactyly Quantitative fluorescent polymerase chain reaction Trisomy 13
Accesso online:	http://www.sciencedirect.com/science/article/pii/S1028455921001923
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