TY  - CHAP
M1  - Book, Section
TI  - Hardcastle Syndrome
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
Y1  - 2019
N1  - 
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
AB  - A  rare  genetic  disorder  characterized  by  skeletal  dysplasia,  diaphyseal  sclerosis,  medullary  stenosis,  pathological  bone  fractures,  and  infarction,  leading  to  malignant  histiocytoma  transformations.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/16
UR  - accesspediatrics.mhmedical.com/content.aspx?aid=1164072144
ER  -