Novel deletion of 6p21.31p21.1 associated with laryngeal cleft, developmental delay, dysmorphic features and vascular anomaly
| Autor: | Pillai, Nishitha R., Marafi, Dana, Monteiro, Sonia A., Parnes, Mered, Chandy, Binoy Mathew, Patel, Ankita, Bacino, Carlos A., Breman, Amy M., Burrage, Lindsay C. |
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| Zdroj: | In European Journal of Medical Genetics June 2019 62(6) |
| Databáze: | ScienceDirect |
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