TY  - CHAP
M1  - Book, Section
TI  - Peutz-Jeghers Syndrome
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
PY  - 2019
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
AB  - A  genetic  disorder  leading  to  congenital  hamartomatous  polyps  of  the  gastrointestinal  tract  associated  with  perioral  melanin  spots.  There  is  an  increased  risk  of  malignancy.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/18
UR  - accesspediatrics.mhmedical.com/content.aspx?aid=1164081576
ER  -