Rare clinical findings in three sporadic cases of Beckwith-Wiedemann syndrome due to novel mutations in the CDKN1C gene

D Jurkiewicz, A Skórka, E Ciara, M Kugaudo… - Clinical …, 2020 - journals.lww.com
Beckwith-Wiedemann syndrome (BWS) is a rare congenital overgrowth disorder
characterised by macroglossia, abdominal wall defects, neonatal hypoglycaemia, lateralised …
被引用次数：7 相关文章

Rare clinical findings in three sporadic cases of Beckwith-Wiedemann syndrome due to novel mutations in the CDKN1C gene

D Jurkiewicz, A Skórka, E Ciara… - Clinical …, 2020 - pubmed.ncbi.nlm.nih.gov
Beckwith-Wiedemann syndrome (BWS) is a rare congenital overgrowth disorder
characterised by macroglossia, abdominal wall defects, neonatal hypoglycaemia, lateralised …

Rare clinical findings in three sporadic cases of Beckwith-Wiedemann syndrome due to novel mutations in the CDKN1C gene.

D Jurkiewicz, A Skórka, E Ciara, M Kugaudo… - Clinical …, 2020 - europepmc.org
Beckwith-Wiedemann syndrome (BWS) is a rare congenital overgrowth disorder
characterised by macroglossia, abdominal wall defects, neonatal hypoglycaemia, lateralised …