Author:
Emison Eileen Sproat,McCallion Andrew S.,Kashuk Carl S.,Bush Richard T.,Grice Elizabeth,Lin Shin,Portnoy Matthew E.,Cutler David J.,Green Eric D.,Chakravarti Aravinda
Publisher
Springer Science and Business Media LLC
Reference42 articles.
1. Bolk, S. et al. A human model for multigenic inheritance: phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locus. Proc. Natl Acad. Sci. USA 97, 268–273 (2000)
2. Gabriel, S. B. et al. Segregation at three loci explains familial and population risk in Hirschsprung disease. Nature Genet. 31, 89–93 (2002)
3. Chakravarti, A. & Lyonnet, S. in The Metabolic and Molecular Bases of Inherited Disease 8th edn (eds Scriver, C. R., Beaudet, A. R., Sly, W. & Valle, D.) Ch. 251, 6231–6255 (McGraw-Hill, New York, 2001)
4. Carrasquillo, M. M. et al. Genome-wide association study and mouse model identify interaction between RET and EDNRB pathways in Hirschsprung disease. Nature Genet. 32, 237–244 (2002)
5. Borrego, S. et al. RET genotypes comprising specific haplotypes of polymorphic variants predispose to isolated Hirschsprung disease. J. Med. Genet. 37, 572–578 (2000)
Cited by
413 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献