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Neuro-Behavioral Phenotype in 16p11.2 Duplication: A Case Series
Duplications of chromosome 16p11.2, even though rare in the general population, are one of the most frequent known genetic causes of autism spectrum disorder and of other neurodevelopmental disorders. However, data about the neuro-behavioral phenotype of these patients are few. We described a sample...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2020
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7603082/ https://www.ncbi.nlm.nih.gov/pubmed/33086486 http://dx.doi.org/10.3390/children7100190 |