Elucidating discrepant results in a prenatal diagnosis of 48,XXY,+18 (Edwards and Klinefelter syndromes)
Author:
Affiliation:
1. Department of Pathology; Medical College of Wisconsin; Milwaukee Wisconsin
2. Wisconsin Diagnostic Laboratories; Milwaukee; Wisconsin
3. Department of Obstetrics and Gynecology; Medical College of Wisconsin; Milwaukee Wisconsin
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference10 articles.
1. DNA sequencing versus standard prenatal aneuploidy screening;Bianchi;N Eng J Med,2014
2. Double aneuploidy with Edwards-Klinefelter syndromes (48,XXY,+18) of maternal origin: Prenatal diagnosis and molecular cytogenetic characterization in a fetus with arthrogryposis of the left wrist and aplasia of the left thumb;Chen;Taiwan J Obstet Gynecol,2011
3. Non-invasive prenatal diagnosis of fetal aneuploidies using massively parallel sequencing-by-ligation and evidence that cell-free fetal DNA in the maternal plasma originates from cytotrophoblastic cells;Faas;Expert Opin Biol Ther,2012
4. Confined placental origin of the circulating cell free fetal DNA revealed by a discordant non-invasive prenatal test result in a trisomy 18 pregnancy;Mao;Clin Chim Acta,2014
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Double aneuploidy: Identification as a result of the discordant fetal sex on placental karyotype and ultrasound;Taiwanese Journal of Obstetrics and Gynecology;2022-11
2. Inaccuracy of non-invasive prenatal screening demands cautious counsel and follow-up;American Journal of Medical Genetics Part A;2015-12-28
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