Rare clinical findings in three sporadic cases of Beckwith-Wiedemann syndrome due to novel mutations in the CDKN1C gene
Dorota Jurkiewicz(Children's Memorial Health Institute), Małgorzata Krajewska‐Walasek(Children's Memorial Health Institute), Magdalena Pelc(Children's Memorial Health Institute), Krystyńa Chrzańowska(University Medical Center Groningen), Monika Kugaudo(University Clinical Centre), Elżbieta Ciara(Children's Memorial Health Institute), Agata Skórka(Medical University of Warsaw)
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