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Journal Abstract Search

111 related items for PubMed ID: 18247312

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  • 3. Mutations in Smad-interacting protein 1 gene are responsible for absence of its expression in Hirschsprung's disease.
    Zhao W, Zhang SC, Huang WK, Li XL.
    Clin Exp Med; 2018 Aug; 18(3):445-451. PubMed ID: 29600337
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  • 4. The single nucleotide polymorphisms in Smad-interacting protein 1 gene contribute to its ectopic expression and susceptibility in Hirschsprung's disease.
    Zhang S, Jiang K, Yuan Z, Wang W.
    Exp Mol Pathol; 2014 Apr; 96(2):219-24. PubMed ID: 24576558
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  • 5. 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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  • 11. Association analysis of the PHOX2B gene with Hirschsprung disease in the Han Chinese population of Southeastern China.
    Liu CP, Li XG, Lou JT, Xue Y, Luo CF, Zhou XW, Chen F, Li X, Li M, Li JC.
    J Pediatr Surg; 2009 Sep; 44(9):1805-11. PubMed ID: 19735829
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  • 12. A review of genetic mutation in familial Hirschsprung's disease in South Africa: towards genetic counseling.
    Moore SW, Zaahl MG.
    J Pediatr Surg; 2008 Feb; 43(2):325-9. PubMed ID: 18280283
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  • 14. [Coding-sequence mutation and polymorphism analysis of EDNRB gene in patients with Hirschsprung's disease from Zhejiang region].
    Zhou MN, Li JC, Ding SP.
    Fen Zi Xi Bao Sheng Wu Xue Bao; 2006 Feb; 39(1):61-5. PubMed ID: 16944573
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  • 15. Mutations in MYOC gene of Indian primary open angle glaucoma patients.
    Mukhopadhyay A, Acharya M, Mukherjee S, Ray J, Choudhury S, Khan M, Ray K.
    Mol Vis; 2002 Nov 15; 8():442-8. PubMed ID: 12447164
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  • 19. Novel nonsense mutation of the endothelin-B receptor gene in a family with Waardenburg-Hirschsprung disease.
    Syrris P, Carter ND, Patton MA.
    Am J Med Genet; 1999 Nov 05; 87(1):69-71. PubMed ID: 10528251
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