Associated Papers
Estimated global prevalence of genetic carriers of hereditary pheochromocytoma-paraganglioma syndrome in a large multiethnic genomic database.
Charoenngam N et al.
European Journal of Endocrinology, 2025
40974092 (PubMed )
Supplement: lvaf191_supplementary_data.docx
RET and PHOX2B genetic polymorphisms and Hirschsprung's disease susceptibility: a meta-analysis.
Liang CM et al.
Plos One, 2014
Genetic variants in RET and risk of Hirschsprung's disease in Southeastern Chinese: a haplotype-based analysis.
Tou J et al.
Bmc Medical Genetics, 2011
Reduced RET expression in gut tissue of individuals carrying risk alleles of Hirschsprung's disease.
Miao X et al.
Human Molecular Genetics, 2010
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