Novel deletion of 6p21.31p21.1 associated with laryngeal...

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European Journal of Medical Genetics 2018 / 8

Novel deletion of 6p21.31p21.1 associated with laryngeal cleft, developmental delay, dysmorphic features and vascular anomaly

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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Language:
english
Journal:
European Journal of Medical Genetics
DOI:
10.1016/j.ejmg.2018.08.012
Date:
August, 2018
File:
PDF, 817 KB
english, 2018
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