Maternal UPD 20 in an infant from a pregnancy with mosaic trisomy 20
Author:
Publisher
Wiley
Subject
Genetics(clinical),Obstetrics and Gynaecology
Reference12 articles.
1. Maternal UPD 20 in a hyperactive child with severe growth retardation
2. Identification of interstitial maternal uniparental disomy (UPD) (14) and complete maternal UPD(20) in a cohort of growth retarded patients
3. 1992. Prenatal diagnosis of chromosomal abnormalities through amniocentesis. In Genetic Disorders and the Fetus: Diagnosis, Prevention, and Treatment, (ed.). Johns Hopkins University Press; Baltimore, MD; 155-210.
4. A revisit of trisomy 20 mosaicism in prenatal diagnosis—an overview of 103 cases
5. Genomic imprinting related to prenatal diagnosis
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1. 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
2. Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic trisomy 20 at amniocentesis in a pregnancy with a favorable outcome;Taiwanese Journal of Obstetrics and Gynecology;2022-01
3. Additional Evidence for Neuropsychiatric Manifestations in Mosaic Trisomy 20: A Case Report and Brief Review;Children;2021-11-10
4. Maternal Uniparental Disomy of Chromosome 20 (UPD(20)mat) as Differential Diagnosis of Silver Russell Syndrome: Identification of Three New Cases;Genes;2021-04-17
5. upd(20)mat is a rare cause of the Silver‐Russell‐syndrome‐like phenotype: Two unrelated cases and screening of large cohorts;Clinical Genetics;2020-03-11
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