Prenatally detected trisomy 20 mosaicism
Author:
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference20 articles.
1. Placental Abruption and Perinatal Mortality in the United States
2. Mitotic errors in somatic cells cause trisomy 21 in about 4.5% of cases and are not associated with advanced maternal age
3. Paternal Uniparental Isodisomy of Chromosome 20q—and the Resulting Changes in GNAS1 Methylation—as a Plausible Cause of Pseudohypoparathyroidism
4. Maternal UPD 20 in a hyperactive child with severe growth retardation
5. Identification of interstitial maternal uniparental disomy (UPD) (14) and complete maternal UPD(20) in a cohort of growth retarded patients
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1. Clinical outcomes of screen-positive genome-wide cfDNA cases for trisomy 20: results from the global expanded NIPT Consortium;Molecular Cytogenetics;2024-04-16
2. Prenatal diagnosis of mosaic chromosomal aneuploidy and uniparental disomy and clinical outcomes evaluation of four fetuses;Molecular Cytogenetics;2023-12-06
3. Prenatal Screening of Cytogenetic Anomalies -A Ten Year Retrospective Study on 1510 Cases;European Journal of Medical and Health Sciences;2023-06-24
4. Clinical utility of chromosomal microarray analysis and whole exome sequencing in foetuses with oligohydramnios;Annals of Medicine;2023-05-27
5. Low-level mosaic trisomy 20 without uniparental disomy 20 at amniocentesis in a pregnancy associated with a favorable outcome, cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes and perinatal progressive decrease of the aneuploid cell line;Taiwanese Journal of Obstetrics and Gynecology;2023-05
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