TY  - CHAP
M1  - Book, Section
TI  - Tel Hashomer Camptodactyly Syndrome
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
PY  - 2019
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
AB  - Genetic  disorder  with  muscular  hypoplasia,  skeletal  anomalies,  increased  creatine  phosphokinase  levels,  and  abnormal  electromyogram.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/16
UR  - accessanesthesiology.mhmedical.com/content.aspx?aid=1164086238
ER  -