Congenital Anomalies and Genetic Associations in Hirschsprung’s Disease
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Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-540-33935-9_9.pdf
Reference199 articles.
1. Alkuraya FS, Lin AE, Irons MB, Kimonis VE (2005) Fryn’s syndrome with Hirschsprung disease: support for possible neural crest involvement. Am J Med Genet A 132:226–230
2. Amiel J, Lyonnet S (2001) Hirschsprung disease, associated syndromes, and genetics: a review. J Med Genet 38:729–739
3. Angrist M, Kauffman E, Slaugenhaupt S, et al (1993) A gene for Hirschsprung disease (megacolon) in the pericentromeric region of human chromosome 10. Nat Genet 4:351–356
4. Angrist M, Bolk S, Halushka M, Lapchak P, Chakravarti A (1996) Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient, Nat Genet 14:341–344
5. Auricchio A, Casari G, Stalano A, Ballabio A (1996) Endothelin-B receptor mutations in patients with isolated Hirschsprung disease from non-inbred populations, Hum Mol Genet 5:351–354
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