Counseling patients with trisomy 17 mosaicism found at genetic amniocentesis
Author:
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference13 articles.
1. 46,XY/47,XY,+17 mosaicism in a newborn with severe malformations
2. Trisomy 17 mosaicism in a four-year seven-month-old white girl: follow-up report
3. Further observations of true mosaic trisomy 17 ascertained in amniotic fluid cell cultures
4. Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studies
Cited by 8 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. Monozygotic twins discordant for low-level mosaic trisomy 17 at amniocentesis in a pregnancy with a favorable outcome and a literature review of heterokaryotypic monozygotic twins at amniocentesis;Taiwanese Journal of Obstetrics and Gynecology;2020-03
2. Prenatal diagnosis of low-level mosaic trisomy 17 with maternal uniparental disomy 17 by amniocentesis in a pregnancy with a favorable outcome;Taiwanese Journal of Obstetrics and Gynecology;2020-03
3. THE RARE REGULAR TRISOMY 17: FREQUENCY AND PHENOTYPIC PORTRAIT;EUREKA: Health Sciences;2017-03-31
4. Mosaic trisomy 17 at amniocentesis: Prenatal diagnosis, molecular genetic analysis, and literature review;Taiwanese Journal of Obstetrics and Gynecology;2016-10
5. Rare case of live born with confirmed mosaic trisomy 17 and review of the literature;Clinical Case Reports;2016-03-16
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