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A single-nucleotide polymorphic variant of the RET proto-oncogene is underrepresented in sporadic Hirschsprung disease
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2000
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Mendelian DisorderGenetic DisorderMedicineGeneticsSporadic Hirschsprung DiseasePathologyMolecular BiologyMolecular GeneticsDisease Gene IdentificationRet Proto-oncogeneMolecular DiagnosticsSingle-nucleotide Polymorphic Variant
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