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Kutkowska-Kaźmierczak A, Boczar M, Kalka E, Castañeda J, Klapecki J, Pietrzyk A, Barczyk A, Malinowska O, Landowska A, Gambin T, et al. Wide Fontanels, Delayed Speech Development and Hoarse Voice as Useful Signs in the Diagnosis of KBG Syndrome: A Clinical Description of 23 Cases with Pathogenic Variants Involving the ANKRD11 Gene or Submicroscopic Chromosomal Rearrangements of 16q24.3. Genes. 2021; 12(8):1257. https://doi.org/10.3390/genes12081257

Kutkowska-Kaźmierczak, Anna, Maria Boczar, Ewa Kalka, Jennifer Castañeda, Jakub Klapecki, Aleksandra Pietrzyk, Artur Barczyk, Olga Malinowska, Aleksandra Landowska, Tomasz Gambin, and et al. 2021. "Wide Fontanels, Delayed Speech Development and Hoarse Voice as Useful Signs in the Diagnosis of KBG Syndrome: A Clinical Description of 23 Cases with Pathogenic Variants Involving the ANKRD11 Gene or Submicroscopic Chromosomal Rearrangements of 16q24.3" Genes 12, no. 8: 1257. https://doi.org/10.3390/genes12081257

Kutkowska-Kaźmierczak, A., Boczar, M., Kalka, E., Castañeda, J., Klapecki, J., Pietrzyk, A., Barczyk, A., Malinowska, O., Landowska, A., Gambin, T., Kowalczyk, K., Wiśniowiecka-Kowalnik, B., Smyk, M., Dawidziuk, M., Niepokój, K., Paczkowska, M., Szyld, P., Lipska-Ziętkiewicz, B., Szczałuba, K., ... Gos, M. (2021). Wide Fontanels, Delayed Speech Development and Hoarse Voice as Useful Signs in the Diagnosis of KBG Syndrome: A Clinical Description of 23 Cases with Pathogenic Variants Involving the ANKRD11 Gene or Submicroscopic Chromosomal Rearrangements of 16q24.3. Genes, 12(8), 1257. https://doi.org/10.3390/genes12081257