Associated Papers
Looking for RET alterations in thyroid cancer: clinical relevance, methodology and timing.
Elisei R et al.
Endocrine, 2023
Actionable genomic variants in 6045 participants from the Qatar Genome Program.
Elfatih A et al.
Human Mutation, 2021
Multiple functional effects of RET kinase domain sequence variants in Hirschsprung disease.
Hyndman BD et al.
Human Mutation, 2013
Functional analysis of the 5' regulatory region of the 5-aminolevulinate synthase (ALAS1) gene in response to estrogen.
du Plessis N et al.
Cellular and Molecular Biology (noisy-le-grand, France), 2009
A review of genetic mutation in familial Hirschsprung's disease in South Africa: towards genetic counseling.
Moore SW et al.
Journal of Pediatric Surgery, 2008
[Molecular biology, basic research and diagnosis of Hirschsprung's disease].
Martucciello G et al.
Der Pathologe, 2007
Familial medullary carcinoma prevention, risk evaluation, and RET in children of families with MEN2.
Moore SW et al.
Journal of Pediatric Surgery, 2007
Novel RET mutations in Hirschsprung's disease patients from the diverse South African population.
Julies MG et al.
European Journal of Human Genetics : Ejhg, 2001
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