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Ocular Manifestations of a Novel Proximal 19p13.3 Microdeletion
Microdeletions at 19p13.3 are rarely reported in the medical literature with significant phenotypic variability. Among the reported cases, common clinical manifestations have included developmental delay, facial dysmorphism, and hypotonia. Herein we described a child with a de novo 19p13.3 microdele...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Hindawi
2018
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5952563/ https://www.ncbi.nlm.nih.gov/pubmed/29854496 http://dx.doi.org/10.1155/2018/2492437 |