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Journal Abstract Search


169 related items for PubMed ID: 17132904

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  • 5. Genetic heterogeneity in Korean families with autosomal-dominant polycystic kidney disease (ADPKD): the first Asian report.
    Lee JG, Lee KB, Kim UK, Ahn C, Hwang DY, Hwang YH, Eo HS, Lee EJ, Kim YS, Han JS, Kim S, Lee JS.
    Clin Genet; 2001 Aug; 60(2):138-44. PubMed ID: 11553048
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  • 6. Characterization of microsatellite markers to diagnose ADPKD.
    Bae Y, Kim H, Paik M, Lee J, Hwang D, Hwang Y, Ahn C, Kang S.
    Mol Cell Probes; 2004 Jun; 18(3):155-9. PubMed ID: 15135448
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  • 8. Genetic analysis of Iranian autosomal dominant polycystic kidney disease: new insight to haplotype analysis.
    Entezam M, Khatami MR, Saddadi F, Ayati M, Roozbeh J, Saghafi H, Keramatipour M.
    Cell Mol Biol (Noisy-le-grand); 2016 Feb 04; 62(2):15-20. PubMed ID: 26950445
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  • 9. Presymptomatic molecular diagnosis of autosomal dominant polycystic kidney disease using PKD1- and PKD2-linked markers in Cypriot families.
    Deltas CC, Christodoulou K, Tjakouri C, Pierides A.
    Clin Genet; 1996 Jul 04; 50(1):10-8. PubMed ID: 8891380
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  • 10. [Gene diagnosis of autosomal dominant polycystic kidney disease type 2 using microsatellite DNA tightly linked to polycystic kidney disease gene 2].
    Zhang WL, Zhang DY, Wu YM, Sun TM, Mei CL.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Aug 04; 21(4):325-8. PubMed ID: 15300626
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  • 11. A family with a milder form of adult dominant polycystic kidney disease not linked to the PKD1 (16p) or PKD2 (4q) genes.
    Ariza M, Alvarez V, Marín R, Aguado S, López-Larrea C, Alvarez J, Menéndez MJ, Coto E.
    J Med Genet; 1997 Jul 04; 34(7):587-9. PubMed ID: 9222969
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  • 12. Bilineal inheritance of pathogenic PKD1 and PKD2 variants in a Czech family with autosomal dominant polycystic kidney disease - a case report.
    Elisakova V, Merta M, Reiterova J, Baxova A, Kotlas J, Hirschfeldova K, Obeidova L, Tesar V, Stekrova J.
    BMC Nephrol; 2018 Jul 04; 19(1):163. PubMed ID: 29973168
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  • 13. Identification of novel mutations and risk assessment of Han Chinese patients with autosomal dominant polycystic kidney disease.
    Zhang M, Liu S, Xia X, Cui Y, Li X.
    Nephrology (Carlton); 2019 May 04; 24(5):504-510. PubMed ID: 29633482
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  • 14. Genotypes of autosomal dominant polycystic kidney disease in Japanese.
    Mizoguchi M, Tamura T, Yamaki A, Higashihara E, Shimizu Y.
    J Hum Genet; 2002 May 04; 47(1):51-4. PubMed ID: 11829141
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  • 15. Identification of novel PKD1 and PKD2 mutations in Korean patients with autosomal dominant polycystic kidney disease.
    Choi R, Park HC, Lee K, Lee MG, Kim JW, Ki CS, Hwang YH, Ahn C.
    BMC Med Genet; 2014 Dec 10; 15():129. PubMed ID: 25491204
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  • 16. Novel PKD1 and PKD2 mutations in autosomal dominant polycystic kidney disease (ADPKD).
    Hoefele J, Mayer K, Scholz M, Klein HG.
    Nephrol Dial Transplant; 2011 Jul 10; 26(7):2181-8. PubMed ID: 21115670
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  • 17. Type identification of autosomal dominant polycystic kidney disease by analysis of fluorescent short tandem repeat markers.
    Lin WD, Wu JY, Tsai FJ, Gau MT, Lee CC.
    J Formos Med Assoc; 2002 Aug 10; 101(8):567-71. PubMed ID: 12440087
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  • 18. Mutation analysis of autosomal dominant polycystic kidney disease genes in Han Chinese.
    Zhang S, Mei C, Zhang D, Dai B, Tang B, Sun T, Zhao H, Zhou Y, Li L, Wu Y, Wang W, Shen X, Song J.
    Nephron Exp Nephrol; 2005 Aug 10; 100(2):e63-76. PubMed ID: 15775720
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  • 19. Comprehensive PKD1 and PKD2 Mutation Analysis in Prenatal Autosomal Dominant Polycystic Kidney Disease.
    Audrézet MP, Corbiere C, Lebbah S, Morinière V, Broux F, Louillet F, Fischbach M, Zaloszyc A, Cloarec S, Merieau E, Baudouin V, Deschênes G, Roussey G, Maestri S, Visconti C, Boyer O, Abel C, Lahoche A, Randrianaivo H, Bessenay L, Mekahli D, Ouertani I, Decramer S, Ryckenwaert A, Cornec-Le Gall E, Salomon R, Ferec C, Heidet L.
    J Am Soc Nephrol; 2016 Mar 10; 27(3):722-9. PubMed ID: 26139440
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  • 20. Mutational screening of PKD1 and PKD2 in Indian ADPKD patients identified 95 genetic variants.
    Raj S, Singh RG, Das P.
    Mutat Res; 2020 Mar 10; 821():111718. PubMed ID: 32823016
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