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Longitudinal report of child with de novo 16p11.2 triplication
16p11.2 deletions and duplications are commonly associated with autism spectrum disorder and linked to mirrored phenotypes of physical characteristics and higher penetrance for deletions. A male with a rare 16p11.2 triplication demonstrated a similar phenotypic presentation to deletion carriers with...
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| Publicado en: | Clin Case Rep |
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| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
John Wiley and Sons Inc.
2017
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5771938/ https://ncbi.nlm.nih.gov/pubmed/29375855 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ccr3.1236 |
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