Associated Papers
Whole exome sequencing approach for identification of the molecular etiology in pediatric patients with hematuria.
Wu J et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2024
[Molecular biology, basic research and diagnosis of Hirschsprung's disease].
Martucciello G et al.
Der Pathologe, 2007
Hirschsprung's disease as a neurochristopathy.
Martucciello G
Pediatric Surgery International, 1997
Mutations of the RET proto-oncogene in the multiple endocrine neoplasia type 2 syndromes, related sporadic tumours, and hirschsprung disease.
Eng C et al.
Human Mutation, 1997
RET mutations in multiple endocrine neoplasia type 2 and Hirschsprung disease.
Reynolds LF et al.
Current Opinion in Pediatrics, 1995
Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung disease.
Attié T et al.
Human Molecular Genetics, 1995
[Mutations of RET proto-oncogene in Hirschsprung disease].
Lyonnet S et al.
Comptes Rendus De L'academie Des Sciences. Serie Iii, Sciences De La Vie, 1994
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