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

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Bibliographic Details
Published in:	Journal of medical genetics 2003-11, Vol.40 (11), p.e122-122
Main Authors:	Garcia-Barceló, M-M, Sham, M-H, Lui, V C-H, Chen, B L-S, Song, Y-Q, Lee, W-S, Yung, S-K, Romeo, G, Tam, P K-H
Format:	Article
Language:	English
Subjects:	Asian Continental Ancestry Group - genetics Births Case-Control Studies China - epidemiology chromosomes not transmitted chromosomes transmitted Electronic Letter Etiology Genes Genetics, Population Genotype Genotype & phenotype Haplotypes Haplotypes - genetics Hardy-Weinberg equilibrium Hirschsprung Disease - epidemiology Hirschsprung Disease - ethnology Hirschsprung Disease - genetics Hirschsprung’s disease Humans HWE Kinases Linkage Disequilibrium - genetics long segment aganglionosis LSA Mutation Oncogene Proteins - genetics Phenotype Polymorphism, Single Nucleotide - genetics Proto-Oncogene Proteins c-ret Receptor Protein-Tyrosine Kinases - genetics RET gene short segment aganglionosis single nucleotide polymorphism SNP SSA TDT Thyroid cancer transmission disequilibrium test
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