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Journal Abstract Search

174 related items for PubMed ID: 10050655

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  • 2. 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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  • 3. Molecular screening of CFTR gene in Egyptian patients with congenital bilateral absence of the vas deferens: a preliminary study.
    Fathy M, Ramzy T, Elmonem MA, Amer M, Zeidan A, Hassan FA, Mehaney DA.
    Andrologia; 2016 Dec; 48(10):1307-1312. PubMed ID: 26989879
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  • 4. Mutation spectrum of the CFTR gene in Taiwanese patients with congenital bilateral absence of the vas deferens.
    Wu CC, Alper OM, Lu JF, Wang SP, Guo L, Chiang HS, Wong LJ.
    Hum Reprod; 2005 Sep; 20(9):2470-5. PubMed ID: 15905293
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  • 7. 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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  • 8. [Detection of pathogenic gene mutations in thirteen cases of congenital bilateral absence of vas deferens infertility patients].
    Tang Y, Zhang Y, Wu D, Lin Y, Lan F.
    Beijing Da Xue Xue Bao Yi Xue Ban; 2024 Oct 18; 56(5):763-774. PubMed ID: 39397452
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  • 12. Mutations in the cystic fibrosis gene in men with congenital bilateral absence of the vas deferens.
    De Braekeleer M, Férec C.
    Mol Hum Reprod; 1996 Sep 18; 2(9):669-77. PubMed ID: 9239681
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  • 13. [Molecular basis of cystic fibrosis and congenital bilateral agenesis of vas deferens].
    Bienvenu T, Claustres M.
    Contracept Fertil Sex; 1996 Jun 18; 24(6):495-500. PubMed ID: 8766513
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  • 17. Increased frequency of CFTR gene mutations identified in Indian infertile men with non-CBAVD obstructive azoospermia and spermatogenic failure.
    Sharma H, Mavuduru RS, Singh SK, Prasad R.
    Gene; 2014 Sep 10; 548(1):43-7. PubMed ID: 25010724
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  • 18. Molecular study of (TG)m(T)n polymorphisms in Iranian males with congenital bilateral absence of the vas deferens.
    Radpour R, Gourabi H, Gilani MA, Dizaj AV.
    J Androl; 2007 Sep 10; 28(4):541-7. PubMed ID: 17314234
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  • 19. CFTR mutations in men with congenital bilateral absence of the vas deferens (CBAVD): a systemic review and meta-analysis.
    Yu J, Chen Z, Ni Y, Li Z.
    Hum Reprod; 2012 Jan 10; 27(1):25-35. PubMed ID: 22081250
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