Molecular Basis of Beckwith–Wiedemann Syndrome Spectrum with Associated Tumors and Consequences for Clinical Practice

SIMPLE SUMMARY: Beckwith–Wiedemann syndrome (BWS, OMIM 130650) is an inborn overgrowth disorder caused by molecular alterations in chromosome 11p15.5. These molecular changes affect so-called imprinted genes, i.e., genes which underlie a complex regulation which is linked to the parental origin of t...

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Detalles Bibliográficos
Autores principales: Eggermann, Thomas, Maher, Eamonn R., Kratz, Christian P., Prawitt, Dirk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9265096/
https://www.ncbi.nlm.nih.gov/pubmed/35804856
http://dx.doi.org/10.3390/cancers14133083

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9265096/
https://www.ncbi.nlm.nih.gov/pubmed/35804856
http://dx.doi.org/10.3390/cancers14133083

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