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Takai, R., Ohta, T. A commentary on de novo MEIS2 mutation causes syndromic developmental delay with persistent gastro-esophageal reflux. J Hum Genet 61, 773–774 (2016). https://doi.org/10.1038/jhg.2016.81
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DOI: https://doi.org/10.1038/jhg.2016.81
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