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Citation: Peyrard-janvid, Myriam et al., Dominant Mutations in GRHL3 Cause Van der Woude Syndrome and Disrupt Oral Periderm Development, American journal of human genetics (Online) AJHG , 94(1), 2013, pp. 23-32

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Citation: Schumacher, Johannes et al., Strong Genetic Evidence of DCDC2 as a Susceptibility Gene for Dyslexia, American journal of human genetics , 78(1), 2006, pp. 52-62