These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
Pubmed for Handhelds
PUBMED FOR HANDHELDS
Search MEDLINE/PubMed
Title: Uniparental disomy and the phenotype of mosaic trisomy 20: a new case and review of the literature. Author: Powis Z, Erickson RP. Journal: J Appl Genet; 2009; 50(3):293-6. PubMed ID: 19638687. Abstract: Mosaic trisomy 20 is one of the most commonly reported chromosome abnormalities detected prenatally, but is rare postnatally. Many studies have hypothesized that uniparental disomy (UPD) may play a role in phenotype variability, but this has not been widely studied. Here we report an additional case of mosaic trisomy 20 with altered pigmentation, in which UPD was not found, and we review the literature.[Abstract] [Full Text] [Related] [New Search]