Mutation analysis of the RET gene in total intestinal aganglionosis by wave DNA fragment analysis system
Author:
Publisher
Elsevier BV
Subject
General Medicine,Pediatrics, Perinatology and Child Health,Surgery
Reference23 articles.
1. Hirschsprung's disease;Puri,1996
2. Nitrergic innervation of the normal gut and in motility disorders of childhood;Rolle;J Pediatr Surg,2002
3. Mutations in SIP1, encoding Smad interacting protein-1, cause a form of Hirschsprung's disease;Wakamatsu;Nat Genet,2001
4. Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung disease;Attie;Hum Mol Genet,1995
5. RET and GDNF gene scanning in Hirschsprung patients using two dual denaturing gel systems;Hofstra;Hum Mutat,2000
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1. Correlation analysis of IL-11 polymorphisms and Hirschsprung disease subtype susceptibility in Southern Chinese Children;BMC Medical Genomics;2021-01-19
2. Total Colonic Aganglionosis and Very-Long-Segment Hirschsprung’s Disease;Hirschsprung's Disease and Allied Disorders;2019
3. A meta-analysis of clinical outcome of intestinal transplantation in patients with total intestinal aganglionosis;Pediatric Surgery International;2017-06-09
4. RET gene is a major risk factor for Hirschsprung’s disease: a meta-analysis;Pediatric Surgery International;2015-07-12
5. Total colonic aganglionosis and Hirschsprung’s disease: a review;Pediatric Surgery International;2014-10-31
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