Additional data on the clinical phenotype of Helsmoortel—Van der Aa syndrome associated with a novel truncating mutation in <i>ADNP</i> gene
Małgorzata Krajewska‐Walasek(Children's Memorial Health Institute), Elżbieta Ciara(Children's Memorial Health Institute), Dorota Piekutowska‐Abramczuk(Children's Memorial Health Institute), Aleksandra Jezela‐Stanek, Krystyńa Chrzańowska(University Medical Center Groningen), Marzena Kucharczyk(Children's Memorial Health Institute), Dorota Jurkiewicz(Children's Memorial Health Institute)
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