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Journal Abstract Search

170 related items for PubMed ID: 19183406

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  • 6. Germline mutations in glial cell line-derived neurotrophic factor (GDNF) and RET in a Hirschsprung disease patient.
    Angrist M, Bolk S, Halushka M, Lapchak PA, Chakravarti A.
    Nat Genet; 1996 Nov; 14(3):341-4. PubMed ID: 8896568
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  • 8. RET and GDNF gene scanning in Hirschsprung patients using two dual denaturing gel systems.
    Hofstra RM, Wu Y, Stulp RP, Elfferich P, Osinga J, Maas SM, Siderius L, Brooks AS, vd Ende JJ, Heydendael VM, Severijnen RS, Bax KM, Meijers C, Buys CH.
    Hum Mutat; 2000 Nov; 15(5):418-29. PubMed ID: 10790203
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  • 9. Within-gene interaction between c.135 G/A genotypes and RET proto-oncogene germline mutations in HSCR families.
    Fitze G, Cramer J, Serra A, Schreiber M, Roesner D, Schackert HK.
    Eur J Pediatr Surg; 2003 Jun; 13(3):152-7. PubMed ID: 12939698
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  • 11. Functional haplotypes of the RET proto-oncogene promoter are associated with Hirschsprung disease (HSCR).
    Fitze G, Appelt H, König IR, Görgens H, Stein U, Walther W, Gossen M, Schreiber M, Ziegler A, Roesner D, Schackert HK.
    Hum Mol Genet; 2003 Dec 15; 12(24):3207-14. PubMed ID: 14600022
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  • 12. Mutational analysis of the RET and GDNF gene in children with hypoganglionosis.
    Inoue K, Shimotake T, Tomiyama H, Iwai N.
    Eur J Pediatr Surg; 2001 Apr 15; 11(2):120-3. PubMed ID: 11371032
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  • 13. A common haplotype at the 5' end of the RET proto-oncogene, overrepresented in Hirschsprung patients, is associated with reduced gene expression.
    Griseri P, Bachetti T, Puppo F, Lantieri F, Ravazzolo R, Devoto M, Ceccherini I.
    Hum Mutat; 2005 Feb 15; 25(2):189-95. PubMed ID: 15643606
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  • 14. Analysis of the RET, GDNF, EDN3, and EDNRB genes in patients with intestinal neuronal dysplasia and Hirschsprung disease.
    Gath R, Goessling A, Keller KM, Koletzko S, Coerdt W, Müntefering H, Wirth S, Hofstra RM, Mulligan L, Eng C, von Deimling A.
    Gut; 2001 May 15; 48(5):671-5. PubMed ID: 11302967
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  • 18. 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 15; 15(2):242-5. PubMed ID: 17091122
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  • 20. Familial associations in medullary thyroid carcinoma with Hirschsprung disease: the role of the RET-C620 "Janus" genetic variation.
    Moore SW, Zaahl M.
    J Pediatr Surg; 2010 Feb 15; 45(2):393-6. PubMed ID: 20152359
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