Trisomy 20 mosaicism caused by a maternal meiosis II error is associated with normal intellect but multiple congenital anomalies
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference13 articles.
1. Trisomy 20 mosaicism in two unrelated girls with skin hypopigmentation and normal intellectual development
2. 1992. Confirmation of true mosaic trisomy 20 in a phenotypically normal liveborn male. Clin Genet 42: 47-49.
3. Maternal UPD 20 in a hyperactive child with severe growth retardation
4. Identification of interstitial maternal uniparental disomy (UPD) (14) and complete maternal UPD(20) in a cohort of growth retarded patients
5. Trisomy 20 mosaicism in prenatal diagnosis–a review and update
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1. Building the brain mosaic: an expanded view;Trends in Genetics;2024-09
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3. 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
4. Further Characterization of Hb Bronovo [α103(G10)His→Leu; HBA2: c.311A>T] and First Report of the Homozygous State;Hemoglobin;2020-05-03
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