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19p13.3 Deletion With Polyotia: A Case Report and Literature Review
Mutations at chromosome 19 are rare, and reports in the literature are scarce and clinically variable. This chromosome has a high genetic density, and hence a given deletion can cause distinctive effects on body systems and, in addition, result in a characteristic phenotype. We report the case of a...
Autores principales: | Silvera Redondo, Carlos, Avendaño Capriles, Camilo Andrés, Fernández Sánchez, David, David Espinosa, Ricardo, Acostamadiedo Marx, Ana Sofía |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8680017/ https://www.ncbi.nlm.nih.gov/pubmed/34976455 http://dx.doi.org/10.7759/cureus.19661 |
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