Mutational analysis ofRET/GDNF/NTN genes in children with total colonic aganglionosis with small bowel involvement
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference41 articles.
1. Mutations of the RET-GDNF Signaling Pathway in Ondine's Curse
2. Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung disease
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4. Germline mosaicism and Duchenne muscular dystrophy mutations
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1. Congenital intestinal stenosis and Hirschsprung’s disease: two extremely rare pathologies in a newborn puppy;BMC Veterinary Research;2019-03-13
2. Total Colonic Aganglionosis and Very-Long-Segment Hirschsprung’s Disease;Hirschsprung's Disease and Allied Disorders;2019
3. Development of the Enteric Nervous System;Physiology of the Gastrointestinal Tract;2018
4. Hemophagocytic lymphohistiocytosis presenting in a pediatric patient with near total colonic and small bowel aganglionosis: a case report;Journal of Medical Case Reports;2017-08-31
5. RET gene is a major risk factor for Hirschsprung’s disease: a meta-analysis;Pediatric Surgery International;2015-07-12
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