TY  - CHAP
M1  - Book, Section
TI  - Meier-Gorlin Syndrome
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
PY  - 2019
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
AB  - It  is  an  inherited  disorder  characterized  by  short  stature,  craniofacial  anomalies,  bilateral  microtia,  and  absence  of  patellae.  Other  clinical  features  include  microstomia,  microcephaly,  hypoplasia  of  the  maxillary,  and  micrognathia.  The  skeletal  anomalies  include  complete  dislocation  of  the  elbow,  hooked  clavicle,  and  clinodactyly.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/19
UR  - accesspediatrics.mhmedical.com/content.aspx?aid=1164078165
ER  -