RET and PHOX2B Genetic Polymorphisms and Hirschsprung's Disease Susceptibility: A Meta-Analysis
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference36 articles.
1. Comprehensive analysis of RET common and rare variants in a series of Spanish Hirschsprung patients confirms a synergistic effect of both kinds of events;R Núñez-Torres;BMC medical genetics,2011
2. Single nucleotide polymorphisms in the RET gene and their correlations with Hirschsprung disease phenotype;R Śmigiel;Journal of applied genetics,2006
3. Association of genetic polymorphisms in the RET-protooncogene and NRG1 with Hirschsprung disease in Thai patients;T Phusantisampan;Journal of human genetics,2012
4. Haplotype analysis reveals a possible founder effect of RET mutation R114H for Hirschsprung's disease in the Chinese population;BK Cornes;PloS one,2010
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1. Association of rs2435357 and rs2506030 polymorphisms in RET with susceptibility to hirschsprung disease: A systematic review and meta-analysis;Frontiers in Pediatrics;2022-10-17
2. Non-polyalanine repeat mutation in PHOX2B is detected in autopsy cases of sudden unexpected infant death;PLOS ONE;2022-04-29
3. Is There Any Mosaicism in REarranged During Transfection Variant in Hirschsprung Disease’s Patients?;Frontiers in Pediatrics;2022-03-10
4. The application of a gamma distribution model to diffusion-weighted images of the orofacial region;Dentomaxillofacial Radiology;2021-02-01
5. APOBEC: A molecular driver in cervical cancer pathogenesis;Cancer Letters;2021-01
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