TY  - CHAP
M1  - Book, Section
TI  - Gorlin-Chaudhry-Moss Syndrome
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
Y1  - 2019
N1  - 
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
AB  - A  very  rare  syndrome  characterized  by  craniosynostosis,  midfacial  hypoplasia,  hypertrichosis,  and  anomalies  of  the  heart  (stenosis  of  the  aortic  and  pulmonary  valves),  eyes,  teeth,  and  external  genitalia.  Mental  retardation  has  been  observed.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/19
UR  - accesspediatrics.mhmedical.com/content.aspx?aid=1164071430
ER  -