Rare clinical findings in three sporadic cases of Beckwith-Wiedemann syndrome due to novel mutations in the CDKN1C gene
Jurkiewicz, Dorota, Skórka, Agata, Ciara, Elżbieta, Kugaudo, Monika, Pelc, Magdalena, Chrzanowska, Krystyna, Krajewska-Walasek, MałgorzataVolume:
29
Journal:
Clinical Dysmorphology
DOI:
10.1097/mcd.0000000000000307
Date:
January, 2020
File:
PDF, 394 KB
2020