Molecular mechanisms ofRET‐induced Hirschsprung pathogenesis
Author:
Publisher
Informa UK Limited
Subject
General Medicine
Link
http://www.tandfonline.com/doi/pdf/10.1080/07853890500442758
Reference51 articles.
1. Total colonic aganglionosis associated with interstitial deletion of the long arm of chromosome 10
2. Close linkage with the RET protooncogene and boundaries of deletion mutations in autosomal dominant Hirschsprung disease
3. Hirschsprung's disease associated with a deletion of chromosome 10 (q11.2q21.2): a further link with the neurocristopathies?
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1. Whole Exome Sequencing Identifies a Novel Pathogenic RET Variant in Hirschsprung Disease;Frontiers in Genetics;2019-01-14
2. Development of the Enteric Neuromuscular System;Pediatric Neurogastroenterology;2016-11-27
3. Clinical and genetic correlations of familial Hirschsprung’s disease;Journal of Pediatric Surgery;2015-02
4. Expression patterns of dishevelled-2 in different colon tissue segments in Hirschsprung’s disease;Molecular Medicine Reports;2014-11-12
5. RET and PHOX2B Genetic Polymorphisms and Hirschsprung's Disease Susceptibility: A Meta-Analysis;PLoS ONE;2014-03-20
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