Dental anomalies as a possible clue of 1p36 deletion syndrome due to germline mosaicism: a case report

BACKGROUND: Monosomy 1p36 is the most common terminal deletion syndrome with an autosomal dominant pattern of inheritance. This syndrome is defined by an extremely wide spectrum of characteristics; however, developmental delay and intellectual disability of various degree are present in all patients...

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Detalles Bibliográficos
Autores principales: Nistico’, D., Guidolin, F., Navarra, C. O., Bobbo, M., Magnolato, A., D’Adamo, A. P., Giorgio, E., Pivetta, B., Barbi, E., Gasparini, P., Cadenaro, M., Sirchia, F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7210666/
https://www.ncbi.nlm.nih.gov/pubmed/32386509
http://dx.doi.org/10.1186/s12887-020-02049-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7210666/
https://www.ncbi.nlm.nih.gov/pubmed/32386509
http://dx.doi.org/10.1186/s12887-020-02049-1

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