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

Journal of medical genetics

Volumn 40, Issue 11, 2003, Pages

  Garcia Barceló, M M ^a   Sham, M H ^a   Lui, V C H ^a   Chen, B L S ^a   Song, Y Q ^a   Lee, W S ^a   Yung, S K ^a   Romeo, G ^a   Tam, P K H ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

ONCOPROTEIN; PROTEIN RET; PROTEIN TYROSINE KINASE; RET PROTEIN, HUMAN;

ARTICLE; ASIAN; CASE CONTROL STUDY; CHINA; COMPARATIVE STUDY; ETHNOLOGY; GENE LINKAGE DISEQUILIBRIUM; GENETICS; GENOTYPE; HAPLOTYPE; HIRSCHSPRUNG DISEASE; HUMAN; PHENOTYPE; POPULATION GENETICS; SINGLE NUCLEOTIDE POLYMORPHISM;

ASIAN CONTINENTAL ANCESTRY GROUP; CASE-CONTROL STUDIES; CHINA; GENETICS, POPULATION; GENOTYPE; HAPLOTYPES; HIRSCHSPRUNG DISEASE; HUMANS; LINKAGE DISEQUILIBRIUM; ONCOGENE PROTEINS; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTO-ONCOGENE PROTEINS C-RET; RECEPTOR PROTEIN-TYROSINE KINASES;

MLCS; MLOWN;

EID: 1542438600     PISSN: None     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.40.11.e122     Document Type: Article

References (0)