TY - CHAP M1 - Book, Section TI - Acromesomelic Dysplasia Type I: Maroteaux Type (AMDM) A1 - Bissonnette, Bruno A1 - Luginbuehl, Igor A1 - Engelhardt, Thomas PY - 2019 T2 - Syndromes: Rapid Recognition and Perioperative Implications, 2e AB - Autosomal recessive. The responsible defect has been linked to mutations of the Natriuretic Peptide Receptor 2 (NPR2) gene on chromosome 9p13-q12. SN - PB - McGraw-Hill Education CY - New York, NY Y2 - 2024/10/03 UR - accesspediatrics.mhmedical.com/content.aspx?aid=1164060545 ER -