Malan syndrome (Sotos syndrome 2) in two patients with 19p13.2 deletion encompassing NFIX gene and novel NFIX sequence variant
Aleksandra Jezela‐Stanek, Małgorzata Krajewska‐Walasek(Children's Memorial Health Institute), Marlena Młynek(Children's Memorial Health Institute), Dorota Wicher(Children's Memorial Health Institute), Rafał Płoski(Medical University of Warsaw), Katarzyna Falana(Warsaw University of Life Sciences), Małgorzata Rydzanicz(Medical University of Warsaw), Elżbieta Ciara(Children's Memorial Health Institute), Marzena Kucharczyk(Children's Memorial Health Institute), Monika Kugaudo(University Clinical Centre), Dorota Jurkiewicz(Children's Memorial Health Institute), Agata Cieślikowska(Children's Memorial Health Institute)
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