Hirschsprung's disease as a neurochristopathy
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/BF01194793.pdf
Reference74 articles.
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2. Angrist M, Bolk S, Thiel B, Puffenberger EG, Hofstra RM, Buys HCM, Cass DT, Chakravarti A (1995) Mutation analysis of the RET receptor tyrosine kinase in Hirschsprung disease. Hum Mol Genet 4: 821–830
3. Attié T, Pelet A, Sarda P, Eng C, Edery P, Mulligan LM, Ponder BAJ, Munnich A, Lyonnet S (1994) A 7 by deletion of the RET proto-oncogene in familial Hirschsprung's disease. Hum Mol Genet 3: 1439–1440
4. Attié T, Pelet A, Edery P, Eng C, Mulligan LM, Amiel J, Boutrand J, Beldijord C, Nihoul-Fèkètè C, Munich A, Ponder BAJ, Lyonnet S (1995) Diversity of RET proto-oncogene mutations in familial and sporadic Hirschprung disease. Hum Mol Genet 4: 1381–1386
5. Badner JA, Chakravarti A (1990) Waardenburg syndrome and Hirschsprung disease: evidence for pleiotropic effects of a single dominant gene. Am J Med Genet 35: 100–104
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