Whole‐exome sequencing identified a variant in EFTUD2 gene in establishing a genetic diagnosis

Overview of attention for article published in Orthodontics & Craniofacial Research, June 2017

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RT @varsome: New EFTUD2 variant https://t.co/2CbQPFkTny linked t facial asymmetry, #micrognathia, choanal atresia & #microcephaly https://t…

Whole-exome sequencing identified a variant in EFTUD2 gene in establishing a genetic diagnosis. https://t.co/FgOiDuDwjH

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