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Journal Abstract Search

210 related items for PubMed ID: 24528961

  • 1. Tissue specific somatic mutations and aganglionosis in Hirschsprung's disease.
    Moore SW, Zaahl MG.
    J Pediatr Surg; 2014 Feb; 49(2):258-61; discussion 261. PubMed ID: 24528961
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  • 2. Clinical and genetic differences in total colonic aganglionosis in Hirschsprung's disease.
    Moore SW, Zaahl M.
    J Pediatr Surg; 2009 Oct; 44(10):1899-903. PubMed ID: 19853744
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  • 5. Clinical and genetic correlations of familial Hirschsprung's disease.
    Moore SW, Zaahl M.
    J Pediatr Surg; 2015 Feb; 50(2):285-8. PubMed ID: 25638620
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  • 6. Incidence of RET mutations in patients with Hirschsprung's disease.
    Sancandi M, Ceccherini I, Costa M, Fava M, Chen B, Wu Y, Hofstra R, Laurie T, Griffths M, Burge D, Tam PK.
    J Pediatr Surg; 2000 Jan; 35(1):139-42; discussion 142-3. PubMed ID: 10646792
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  • 8. Long segment and short segment familial Hirschsprung's disease: variable clinical expression at the RET locus.
    Edery P, Pelet A, Mulligan LM, Abel L, Attié T, Dow E, Bonneau D, David A, Flintoff W, Jan D.
    J Med Genet; 1994 Aug; 31(8):602-6. PubMed ID: 7815416
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  • 11. RET gene is a major risk factor for Hirschsprung's disease: a meta-analysis.
    Tomuschat C, Puri P.
    Pediatr Surg Int; 2015 Aug; 31(8):701-10. PubMed ID: 26164711
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  • 15. Discrepancy between macroscopic and microscopic transitional zones in Hirschsprung's disease with reference to the type of RET/GDNF/SOX10 gene mutation.
    Shimotake T, Tomiyama H, Aoi S, Iwai N.
    J Pediatr Surg; 2003 May; 38(5):698-701. PubMed ID: 12720173
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  • 16. A novel Czech kindred with familial medullary thyroid carcinoma and Hirschsprung's disease.
    Dvoráková S, Dvoráková K, Malíková M, Skába R, Vlcek P, Bendlová B.
    J Pediatr Surg; 2005 Jun; 40(6):e1-6. PubMed ID: 15991157
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  • 17. Hirschsprung's disease as a model of complex genetic etiology.
    Borrego S, Ruiz-Ferrer M, Fernández RM, Antiñolo G.
    Histol Histopathol; 2013 Sep; 28(9):1117-36. PubMed ID: 23605783
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  • 19. Association between c135G/A genotype and RET proto-oncogene germline mutations and phenotype of Hirschsprung's disease.
    Fitze G, Cramer J, Ziegler A, Schierz M, Schreiber M, Kuhlisch E, Roesner D, Schackert HK.
    Lancet; 2002 Apr 06; 359(9313):1200-5. PubMed ID: 11955539
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  • 20. Allele dosage-dependent penetrance of RET proto-oncogene in an Israeli-Arab inbred family segregating Hirschsprung disease.
    Basel-Vanagaite L, Pelet A, Steiner Z, Munnich A, Rozenbach Y, Shohat M, Lyonnet S.
    Eur J Hum Genet; 2007 Feb 06; 15(2):242-5. PubMed ID: 17091122
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