RT Book, Section
A1 Bissonnette, Bruno
A1 Luginbuehl, Igor
A1 Engelhardt, Thomas
SR Print(0)
ID 1164075654
T1 Korula-Wilson-Salomon Syndrome
T2 Syndromes: Rapid Recognition and Perioperative Implications, 2e
YR 2019
FD 2019
PB McGraw-Hill Education
PP New York, NY
SN 9781259861789
LK accesspediatrics.mhmedical.com/content.aspx?aid=1164075654
RD 2024/04/18
AB It  is  an  inherited  medical  condition  characterized  by  facial  features  such  as  incomplete  closure  of  eyelids,  cleft  lip/palate,  and  hypodontia.,  the  existence  of  which,  as  a  separate  entity,  is  questionable.