TY  - CHAP
M1  - Book, Section
TI  - Sensenbrenner Syndrome
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
Y1  - 2019
N1  - 
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
AB  - Ciliopathy.  Autosomal  recessive  disorder  characterized  by  dolichocephaly,  sagittal  suture  synostosis,  sparse  and  slow-growing  fine  hair,  hypertelorism,  nystagmus,  taurodontia,  dental  fusion,  anteverted  nares,  brachydactyly,  clinodactyly,  narrow  thorax  leading  to  respiratory  problems,  and  mild  mental  retardation.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/17
UR  - accessanesthesiology.mhmedical.com/content.aspx?aid=1164084913
ER  -