TY - CHAP M1 - Book, Section TI - Chondrodysplasia Grebe Type A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas Y1 - 2019 N1 - T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - A rare form of autosomal recessive osteochondrodysplasia characterized by severe dwarfism with marked hypomelia and deformation. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/10/08 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164065546 ER -