Chinese patients with sporadic Hirschsprung's disease are predominantly represented by a single RET haplotype

J Med Genet. 2003 Nov;40(11):e122. doi: 10.1136/jmg.40.11.e122.
No abstract available

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Asian People / genetics
  • Case-Control Studies
  • China / epidemiology
  • Genetics, Population
  • Genotype
  • Haplotypes / genetics*
  • Hirschsprung Disease / epidemiology*
  • Hirschsprung Disease / ethnology
  • Hirschsprung Disease / genetics*
  • Humans
  • Linkage Disequilibrium / genetics
  • Oncogene Proteins / genetics*
  • Phenotype
  • Polymorphism, Single Nucleotide / genetics
  • Proto-Oncogene Proteins c-ret
  • Receptor Protein-Tyrosine Kinases / genetics*

Substances

  • Oncogene Proteins
  • Proto-Oncogene Proteins c-ret
  • RET protein, human
  • Receptor Protein-Tyrosine Kinases