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Haploinsufficiency of novel FOXG1B variants in a patient with severe mental retardation, brain malformations and microcephaly
Sarah A Shoichet, Stella-Amrei Kunde, Petra Viertel, Can Schell-Apacik, Hubertus von Voss, Niels Tommerup, Hans-Hilger Ropers, Vera M Kalscheuer