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Journal Abstract Search

238 related items for PubMed ID: 22103471

  • 1. Molecular screening of the CFTR gene in Mexican patients with congenital absence of the vas deferens.
    Saldaña-Alvarez Y, Jiménez-Morales S, Echevarría-Sánchez M, Jiménez-Ruíz JL, García-Cavazos R, Velázquez-Cruz R, Carnevale A, Orozco L.
    Genet Test Mol Biomarkers; 2012 Apr; 16(4):292-6. PubMed ID: 22103471
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  • 2. A Survey of the Common Mutations and IVS8-Tn Polymorphism of Cystic Fibrosis Transmembrane Conductance Regulator Gene in Infertile Men with Nonobstructive Azoospermia and CBAVD in Iranian Population.
    Asadi F, Mirfakhraie R, Mirzajani F, Khedri A.
    Iran Biomed J; 2019 Mar; 23(2):92-8. PubMed ID: 29986553
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  • 3. 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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  • 4. Prevalence of CBAVD in azoospermic men carrying pathogenic CFTR mutations - Evaluated in a cohort of 639 non-vasectomized azoospermic men.
    Fedder J, Jørgensen MW, Engvad B.
    Andrology; 2021 Mar 10; 9(2):588-598. PubMed ID: 33095972
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  • 10. 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 10; 12(7):469-73. PubMed ID: 16714368
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  • 11. Correlation between CFTR gene mutations in Iranian men with congenital absence of the vas deferens and anatomical genital phenotype.
    Radpour R, Gourabi H, Gilani MA, Dizaj AV.
    J Androl; 2008 Jul 10; 29(1):35-40. PubMed ID: 17673436
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  • 20. Two novel missense and one novel nonsense CFTR mutations in Iranian males with congenital bilateral absence of the vas deferens.
    Radpour R, Gourabi H, Gilani MA, Dizaj AV, Rezaee M, Mollamohamadi S.
    Mol Hum Reprod; 2006 Nov 10; 12(11):717-21. PubMed ID: 16973827
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