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  - 2024/04/20
UR  - accesspediatrics.mhmedical.com/content.aspx?aid=1164060545
ER  -