Maxillo-Facial Morphology in Beckwith-Wiedemann Syndrome: A Preliminary Study on (epi)Genotype-Phenotype Association in Caucasians

Beckwith–Wiedemann syndrome (BWS) is a congenital overgrowth disorder caused by various (epi)genetic alterations affecting the expression of genes on chromosome 11p15. Cardinal features include abdominal wall defects, macroglossia, and cancer predisposition. Several (epi)genotype–phenotype associati...

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Detalles Bibliográficos
Autores principales: Defabianis, Patrizia, Mussa, Alessandro, Ninivaggi, Rossella, Carli, Diana, Romano, Federica
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8872180/
https://www.ncbi.nlm.nih.gov/pubmed/35206635
http://dx.doi.org/10.3390/ijerph19042448

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8872180/
https://www.ncbi.nlm.nih.gov/pubmed/35206635
http://dx.doi.org/10.3390/ijerph19042448

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