Derivation and investigation of the first human cell-based model of Beckwith-Wiedemann syndrome

Genomic imprinting is a rare form of gene expression in mammals in which a small number of genes are expressed in a parent-of-origin-specific manner. The aetiology of human imprinting disorders is diverse and includes chromosomal abnormalities, mutations, and epigenetic dysregulation of imprinted ge...

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Main Authors:	Suhee Chang, Stella K. Hur, Natali S. Sobel Naveh, Joanne L. Thorvaldsen, Deborah L. French, Alyssa L Gagne, Chintan D. Jobaliya, Montserrat C. Anguera, Marisa S. Bartolomei, Jennifer M Kalish
Format:	Artigo
Language:	Inglês
Published:	Taylor & Francis Group 2021-12-01
Series:	Epigenetics
Subjects:	beckwith-wiedemann syndrome induced pluripotent stem cells imprinting
Online Access:	http://dx.doi.org/10.1080/15592294.2020.1861172
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