Paternal uniparental disomy with segmental loss of heterozygosity of chromosome 11 are hallmark characteristics of syndromic and sporadic embryonal rhabdomyosarcoma

In this study, we are able to clearly demonstrate complete UPD11 in both syndromic and sporadic ERMS. © 2016 Wiley Periodicals, Inc.

Source: American Journal of Medical Genetics Part A - August 31, 2016 Category: Genetics & Stem Cells Authors: Katherine M. Robbins, Deborah L. Stabley, Jennifer Holbrook, Rebecca Sahraoui, Alexa Sadreameli, Katrina Conard, Laura Baker, Karen W. Gripp, Katia Sol ‐Church Tags: Original Article Source Type: research