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207 related items for PubMed ID: 30214069

  • 1. CFTR variants and renal abnormalities in males with congenital unilateral absence of the vas deferens (CUAVD): a systematic review and meta-analysis of observational studies.
    Cai H, Qing X, Niringiyumukiza JD, Zhan X, Mo D, Zhou Y, Shang X.
    Genet Med; 2019 Apr; 21(4):826-836. PubMed ID: 30214069
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  • 3. Cystic fibrosis transmembrane conductance regulator (CFTR) gene abnormalities in Indian males with congenital bilateral absence of vas deferens & renal anomalies.
    Gajbhiye R, Kadam K, Khole A, Gaikwad A, Kadam S, Shah R, Kumaraswamy R, Khole V.
    Indian J Med Res; 2016 May; 143(5):616-23. PubMed ID: 27488005
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  • 4. Significance of CFTR gene mutations in patients with congenital aplasia of vas deferens with special regard to renal aplasia.
    Schwarzer JU, Schwarz M.
    Andrologia; 2012 Oct; 44(5):305-7. PubMed ID: 22340520
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  • 5. Characterization of cystic fibrosis conductance transmembrane regulator gene mutations and IVS8 poly(T) variants in Portuguese patients with congenital absence of the vas deferens.
    Grangeia A, Niel F, Carvalho F, Fernandes S, Ardalan A, Girodon E, Silva J, Ferrás L, Sousa M, Barros A.
    Hum Reprod; 2004 Nov; 19(11):2502-8. PubMed ID: 15333598
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  • 6. Genetic, andrological and clinical characteristics of patients with congenital bilateral absence of the vas deferens.
    Attardo T, Vicari E, Mollica F, Grazioso C, Burrello N, Garofalo MR, Lizzio MN, Garigali G, Cannizzaro M, Ruvolo G, D'Agata R, Calogero AE.
    Int J Androl; 2001 Apr; 24(2):73-9. PubMed ID: 11298840
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  • 11. Expanding the phenotypic and genetic spectrum of Chinese patients with congenital absence of vas deferens bearing CFTR and ADGRG2 alleles.
    Yuan P, Liang ZK, Liang H, Zheng LY, Li D, Li J, Zhang J, Tian J, Lai LH, Zhang K, He ZY, Zhang QX, Wang WJ.
    Andrology; 2019 May; 7(3):329-340. PubMed ID: 30811104
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  • 12. Heterogenous spectrum of CFTR gene mutations in Indian patients with congenital absence of vas deferens.
    Sharma N, Acharya N, Singh SK, Singh M, Sharma U, Prasad R.
    Hum Reprod; 2009 May; 24(5):1229-36. PubMed ID: 19181743
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  • 13. Molecular analysis of the IVS8-T splice variant 5T and M470V exon 10 missense polymorphism in Iranian males with congenital bilateral absence of the vas deferens.
    Radpour R, Gilani MA, Gourabi H, Dizaj AV, Mollamohamadi S.
    Mol Hum Reprod; 2006 Jul; 12(7):469-73. PubMed ID: 16714368
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  • 14. Heterogeneous spectrum of mutations in CFTR gene from Indian patients with congenital absence of the vas deferens and their association with cystic fibrosis genetic modifiers.
    Sharma H, Mavuduru RS, Singh SK, Prasad R.
    Mol Hum Reprod; 2014 Sep; 20(9):827-35. PubMed ID: 24958810
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  • 15. Extensive analysis of 40 infertile patients with congenital absence of the vas deferens: in 50% of cases only one CFTR allele could be detected.
    Casals T, Bassas L, Ruiz-Romero J, Chillón M, Giménez J, Ramos MD, Tapia G, Narváez H, Nunes V, Estivill X.
    Hum Genet; 1995 Feb; 95(2):205-11. PubMed ID: 7532150
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  • 16. [Association of CFTR gene polymorphism with congenital bilateral absence of vas deferens in ethnic Han Chinese patients].
    Liu LJ, Li HG, Gu X, Zhu JW, Zhao K, Tang YP, Xiong CL.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Dec; 30(6):729-32. PubMed ID: 24327157
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  • 17. Congenital bilateral absence of the vas deferens: clinical characteristics, biological parameters, cystic fibrosis transmembrane conductance regulator gene mutations, and implications for genetic counseling.
    Daudin M, Bieth E, Bujan L, Massat G, Pontonnier F, Mieusset R.
    Fertil Steril; 2000 Dec; 74(6):1164-74. PubMed ID: 11119745
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