Prenatal diagnosis of low-level mosaicism for trisomy 21 with rare karyotype detected by noninvasive prenatal testing
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynaecology
Reference5 articles.
1. Chromosome 21 and down syndrome: from genomics to pathophysiology;Antonarakis;Nat Rev Genet,2004
2. The neuropsychology of down syndrome: evidence for hippocampal dysfunction;Pennington;Child Dev,2003
3. DNA sequencing of maternal plasma to identify down syndrome and other trisomies in multiple gestations;Canick;Prenat Diagn,2012
4. Postnatal identification of trisomy 21: an overview of 7,133 postnatal trisomy 21 cases identified in a diagnostic reference laboratory in China;Zhao;PLoS One,2015
5. Prenatal diagnosis and molecular cytogenetic characterization of low-level true mosaicism for trisomy 21 using uncultured amniocytes;Chen;Taiwan J Obstet Gynecol,2016
Cited by 4 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. Prenatal diagnosis of maternal uniparental disomy 21 in association with low-level mosaic trisomy 21 at amniocentesis in a pregnancy associated with intrauterine growth restriction and a favorable outcome;Taiwanese Journal of Obstetrics and Gynecology;2022-01
2. Analysis of genetic characteristics of 436 children with dysplasia and detailed analysis of rare karyotype;Open Life Sciences;2022-01-01
3. Prenatal diagnosis of low-level mosaicism for trisomy 21 by amniocentesis in a pregnancy associated with maternal uniparental disomy of chromosome 21 in the fetus and a favorable outcome;Taiwanese Journal of Obstetrics and Gynecology;2020-09
4. Perinatal cytogenetic discrepancy in a fetus with low-level mosaicism for trisomy 21 and a favorable outcome;Taiwanese Journal of Obstetrics and Gynecology;2020-05
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