TY  - CHAP
M1  - Book, Section
TI  - Muller Barth Menger Syndrome
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
PY  - 2019
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
AB  - It  is  a  genetic  disease  characterized  by  the  presence  of  multiple  cerebral  malformation,  seizures,  hypertrichosis,  distinct  face,  claw  hands,  and  overlapping  fingers.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/20
UR  - accessanesthesiology.mhmedical.com/content.aspx?aid=1164079502
ER  -