Low-level mosaic trisomy 2 at amniocentesis in a pregnancy associated with positive NIPT and CVS results for trisomy 2, maternal uniparental disomy 2, perinatal progressive decrease of the aneuploid cell line, cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes, intrauterine growth restriction and a favorable fetal outcome
Author:
Funder
National Science and Technology Council
Ministry of Science and Technology, Taiwan
Publisher
Elsevier BV
Subject
Obstetrics and Gynecology
Reference17 articles.
1. Prenatal diagnosis of mosaic trisomy 2: discrepancy between molecular cytogenetic analyses of uncultured amniocytes and karyotyping of cultured amniocytes in a pregnancy with severe fetal intrauterine growth restriction;Chen;Taiwan J Obstet Gynecol,2011
2. Mosaic trisomy 2 at amniocentesis: prenatal diagnosis and molecular genetic analysis;Chen;Taiwan J Obstet Gynecol,2012
3. Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly and facial dysmorphism;Chen;Taiwan J Obstet Gynecol,2013
4. Prenatal diagnosis of low-level mosaicism for trisomy 2 associated with a favorable pregnancy outcome;Chen;Taiwan J Obstet Gynecol,2016
5. Prenatal diagnosis of mosaicism for trisomy 2 in a single colony at amniocentesis in a pregnancy with a favorable outcome;Chen;Taiwan J Obstet Gynecol,2017
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