Identification of a DNA Methylation Episignature in the 22q11.2 Deletion Syndrome

The 22q11.2 deletion syndrome (22q11.2DS) is the most common genomic disorder in humans and is the result of a recurrent 1.5 to 2.5 Mb deletion, encompassing approximately 20–40 genes, respectively. The clinical presentation of the typical deletion includes: Velocardiofacial, Di George, Opitz G/BBB...

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Detalles Bibliográficos
Autores principales: Rooney, Kathleen, Levy, Michael A., Haghshenas, Sadegheh, Kerkhof, Jennifer, Rogaia, Daniela, Tedesco, Maria Giovanna, Imperatore, Valentina, Mencarelli, Amedea, Squeo, Gabriella Maria, Di Venere, Eleonora, Di Cara, Giuseppe, Verrotti, Alberto, Merla, Giuseppe, Tedder, Matthew L., DuPont, Barbara R., Sadikovic, Bekim, Prontera, Paolo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8395258/
https://www.ncbi.nlm.nih.gov/pubmed/34445317
http://dx.doi.org/10.3390/ijms22168611

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8395258/
https://www.ncbi.nlm.nih.gov/pubmed/34445317
http://dx.doi.org/10.3390/ijms22168611

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