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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1997 | 1 |
1999 | 1 |
2007 | 1 |
2008 | 1 |
2010 | 1 |
2024 | 0 |
PubMed (cited) for id: 613712
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New roles of EDNRB and EDN3 in the pathogenesis of Hirschsprung disease.
Genet Med. 2010 Jan;12(1):39-43. doi: 10.1097/GIM.0b013e3181c371b0.
Genet Med. 2010.
PMID: 20009762
Free article.
Hirschsprung disease, associated syndromes and genetics: a review.
Amiel J, Sproat-Emison E, Garcia-Barcelo M, Lantieri F, Burzynski G, Borrego S, Pelet A, Arnold S, Miao X, Griseri P, Brooks AS, Antinolo G, de Pontual L, Clement-Ziza M, Munnich A, Kashuk C, West K, Wong KK, Lyonnet S, Chakravarti A, Tam PK, Ceccherini I, Hofstra RM, Fernandez R; Hirschsprung Disease Consortium.
Amiel J, et al.
J Med Genet. 2008 Jan;45(1):1-14. doi: 10.1136/jmg.2007.053959. Epub 2007 Oct 26.
J Med Genet. 2008.
PMID: 17965226
Review.
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A heterozygous frameshift mutation in the endothelin-3 (EDN-3) gene in isolated Hirschsprung's disease.
Svensson PJ, Von Tell D, Molander ML, Anvret M, Nordenskjöld A.
Svensson PJ, et al.
Pediatr Res. 1999 May;45(5 Pt 1):714-7. doi: 10.1203/00006450-199905010-00018.
Pediatr Res. 1999.
PMID: 10231870
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Endothelin-3 gene mutations in isolated and syndromic Hirschsprung disease.
Bidaud C, Salomon R, Van Camp G, Pelet A, Attié T, Eng C, Bonduelle M, Amiel J, Nihoul-Fékété C, Willems PJ, Munnich A, Lyonnet S.
Bidaud C, et al.
Eur J Hum Genet. 1997 Jul-Aug;5(4):247-51.
Eur J Hum Genet. 1997.
PMID: 9359047
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