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Deletion Syndrome 22q11.2: A Systematic Review
22q11.2 deletion syndrome (DS 22q11.2) is a rare disease of genetic origin, caused by the loss of the q11.2 region of chromosome 22. It affects one in 4000 live newborns, and among the clinical manifestations that can occur in this syndrome are abnormalities in the parathyroid glands (producing calc...
Autores principales: | Cortés-Martín, Jonathan, Peñuela, Nuria López, Sánchez-García, Juan Carlos, Montiel-Troya, Maria, Díaz-Rodríguez, Lourdes, Rodríguez-Blanque, Raquel |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9406687/ https://www.ncbi.nlm.nih.gov/pubmed/36010058 http://dx.doi.org/10.3390/children9081168 |
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