The contribution of associated congenital anomalies in understanding Hirschsprung’s disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Surgery,Pediatrics, Perinatology, and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s00383-006-1655-2.pdf
Reference161 articles.
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2. Bolk S, Pelet A, Hofstra RM, Angrist M, Salomon R, Croaker D et al (2000) 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(1):268–273
3. Amiel J, Lyonnet S ( 2001) Hirschsprung disease, associated syndromes, and genetics: a review. J Med Genet 38(11):729–739
4. Carrasquillo MM, McCallion AS, Puffenberger EG, Kaschuk CS, No N, Chakravarti A (2002) Genome-wide association study as well as the study of mouse models help to identify the interaction between RET and EDNRB pathways in Hirschsprung disease. Nat Genet 32:237–244
5. Passarge E (1967) The genetics of Hirschsprung disease. N Engl J Med 276:138–143
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