Clinical and genetic correlations of familial Hirschsprung’s disease
Author:
Publisher
Elsevier BV
Subject
General Medicine,Pediatrics, Perinatology, and Child Health,Surgery
Reference34 articles.
1. Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung disease;Attie;Hum Mol Genet,1995
2. Hirschsprung disease, associated syndromes, and genetics: a review;Amiel;J Med Genet,2001
3. The contribution of associated congenital anomalies in understanding Hirschsprungs disease;Moore;Pediatr Surg Int,2006
4. Chromosomal and related Mendelian syndromes associated with Hirschsprungs disease;Moore;Pediatr Surg Int,2012
5. Genome-wide association study as well as the study of mouse models help to identify the interaction between RET and EDNRB pathways in Hirschsprung disease;Carrasquillo;Nat Genet,2002
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4. Novel Causative RET Mutation in a Japanese Family with Hirschsprung's Disease: Case Report and Factors Impacting Disease Severity;Journal of Pediatric Genetics;2020-10-05
5. Enfermedad de Hirschsprung;EMC - Pediatría;2019-08
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