TY - CHAP M1 - Book, Section TI - SC Phocomelia Syndrome A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - A very rare, autosomal recessive, severe, polymalformative disease characterized by cranial and maxillofacial deformities, limb anomalies, and intellectual disability. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/03/28 UR - accessanesthesiology.mhmedical.com/content.aspx?aid=1164084421 ER -