Trisomy 17 mosaicism in amniotic fluid cells not found at birth in blood but present in skin fibroblasts
Author:
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference10 articles.
1. 46,XY/47,XY,+17 mosaicism in a newborn with severe malformations
2. Trisomy 17 detected in amniotic fluid cells but not in newborn infant
3. Prezygotic origin of the isochromosome 12p in Pallister-Killian syndrome
4. Mosaic trisomy 17 in amniotic fluid cells not confirmed in the newborn
5. RARE TRISOMY MOSAICISM DIAGNOSED IN AMNIOCYTES, INVOLVING AN AUTOSOME OTHER THAN CHROMOSOMES 13, 18, 20, AND 21: KARYOTYPE/PHENOTYPE CORRELATIONS
Cited by 18 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. A case report of trisomy 17 mosaicism: PMP22 gene duplication as a result of trisomy 17 associated with Charcot-Marie-Tooth disease;Clinical Dysmorphology;2020-01
4. THE RARE REGULAR TRISOMY 17: FREQUENCY AND PHENOTYPIC PORTRAIT;EUREKA: Health Sciences;2017-03-31
5. Mosaic trisomy 17 at amniocentesis: Prenatal diagnosis, molecular genetic analysis, and literature review;Taiwanese Journal of Obstetrics and Gynecology;2016-10
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