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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...
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. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
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 |
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