Role of RET and ko=PHOX2B gene polymorphisms in risk of Hirschsprung's disease in Chinese population
Open Access
- 1 May 2007
- Vol. 56 (5), 736
- https://doi.org/10.1136/gut.2006.116145
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- An In Vitro Approach to Test the Possible Role of Candidate Factors in the Transcriptional Regulation of the RET Proto-OncogeneGene Expression, 2005
- Studying the genetics of Hirschsprung's disease: unraveling an oligogenic disorderClinical Genetics, 2004
- TTF-1 and RET promoter SNPs: regulation of RET transcription in Hirschsprung's diseaseHuman Molecular Genetics, 2004
- Chinese patients with sporadic Hirschsprung's disease are predominantly represented by a single RET haplotypeJournal of Medical Genetics, 2003
- Hirschsprung Disease Is Linked to Defects in Neural Crest Stem Cell FunctionScience, 2003
- Association study of PHOX2B as a candidate gene for Hirschsprung's diseaseGut, 2003
- Epidemiologic methods: the “art” in the state of the artJournal of Clinical Epidemiology, 2002
- Hirschsprung disease, associated syndromes, and genetics: a reviewJournal of Medical Genetics, 2001
- The homeobox gene Phox2b is essential for the development of autonomic neural crest derivativesNature, 1999
- A gene for Hirschsprung disease (megacolon) in the pericentromeric region of human chromosome 10Nature Genetics, 1993