Novel familial distal imprinting centre 1 (11p15.5) deletion provides further insights in imprinting regulation

BACKGROUND: Deletions of the imprinting centre 1 (IC1) in 11p15.5 are rare and their clinical significance is not only influenced by their parental origin but also by their exact genomic localization. In case the maternal IC1 allele is affected, the deletion is associated with the overgrowth disorde...

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Detalles Bibliográficos
Autores principales: Kraft, Florian, Wesseler, Katharina, Begemann, Matthias, Kurth, Ingo, Elbracht, Miriam, Eggermann, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6377752/
https://www.ncbi.nlm.nih.gov/pubmed/30770769
http://dx.doi.org/10.1186/s13148-019-0629-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6377752/
https://www.ncbi.nlm.nih.gov/pubmed/30770769
http://dx.doi.org/10.1186/s13148-019-0629-x

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