TY - CHAP M1 - Book, Section TI - Korula-Wilson-Salomon Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas Y1 - 2019 N1 - T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e 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. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164075654 ER -