Associated Papers
Functional analyses of RET mutations in Chinese Hirschsprung disease patients.
Leon TY et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology, 2012
Highly recurrent RET mutations and novel mutations in genes of the receptor tyrosine kinase and endothelin receptor B pathways in Chinese patients with sporadic Hirschsprung disease.
Garcia-Barceló M et al.
Clinical Chemistry, 2004
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