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Dentofacial characteristics in a child with Meier–Gorlin syndrome: A rare case report
Meier–Gorlin syndrome (MGS) is a rare autosomal recessive disorder characterized by the triad of microtia, absent or small patellae and short stature. The other associated clinical features may include developmental delay, congenital pulmonary emphysema, gastro-esophageal reflux, urogenital anomalie...
Autores principales: | Morankar, Rahul G., Goyal, Ashima, Gauba, Krishan, Kapur, Aditi |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6011216/ https://www.ncbi.nlm.nih.gov/pubmed/29942112 http://dx.doi.org/10.1016/j.sdentj.2018.04.004 |
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