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Journal Abstract Search

197 related items for PubMed ID: 29986553

  • 1.
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  • 2. 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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  • 3. 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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  • 6. [Mutations and polymorphisms in CFTR genes in infertile men with oligospermia or azoospermia].
    Kusić J, Radojković D, Maletić V, Branković S, Savić A.
    Srp Arh Celok Lek; 2002 Jul 10; 130(1-2):1-6. PubMed ID: 12073281
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  • 7. The prevalence of common CFTR mutations in Iranian infertile men with non-CAVD obstructive azoospermia by using ARMS PCR techniques.
    Safinejad K, Darbouy M, Kalantar SM, Zeinali S, Mirfakhraie R, Yadegar L, Houshmand M.
    J Assist Reprod Genet; 2011 Nov 10; 28(11):1087-90. PubMed ID: 21976147
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  • 9. 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 10; 143(5):616-23. PubMed ID: 27488005
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  • 11. 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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  • 13. Genetic diagnosis and sperm retrieval outcomes for Chinese patients with congenital bilateral absence of vas deferens.
    Wang H, An M, Liu Y, Hu K, Jin Y, Xu S, Chen B, Lu M.
    Andrology; 2020 Sep 10; 8(5):1064-1069. PubMed ID: 32020786
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  • 14. The role of SLC9A3 in Taiwanese patients with congenital bilateral absence of vas deferens (CBAVD).
    Chiang HS, Wang YY, Lin YH, Wu YN.
    J Formos Med Assoc; 2019 Dec 10; 118(12):1576-1583. PubMed ID: 30797621
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  • 15. Cystic fibrosis transmembrane conductance regulator mutations and polymorphisms associated with congenital bilateral absence of vas deferens in a restricted group of patients from North Africa.
    Boudaya M, Fredj SH, Haj RB, Khrouf M, Bouker A, Halouani L, Messaoud T.
    Ann Hum Biol; 2012 Jan 10; 39(1):76-9. PubMed ID: 22148899
    [Abstract] [Full Text] [Related]

  • 16. [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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  • 18. Proportion of cystic fibrosis gene mutations not detected by routine testing in men with obstructive azoospermia.
    Mak V, Zielenski J, Tsui LC, Durie P, Zini A, Martin S, Longley TB, Jarvi KA.
    JAMA; 1999 Jun 16; 281(23):2217-24. PubMed ID: 10376575
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  • 19. Cystic fibrosis mutation screening in CBAVD patients and men with obstructive azoospermia or severe oligozoospermia.
    Kanavakis E, Tzetis M, Antoniadi T, Pistofidis G, Milligos S, Kattamis C.
    Mol Hum Reprod; 1998 Apr 16; 4(4):333-7. PubMed ID: 9620832
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  • 20. The detection and significance of cystic fibrosis transmembrane conductance regulator gene promoter mutations in Chinese patients with congenital bilateral absence of the vas deferens.
    Bai S, Du Q, Liu X, Tong Y, Wu B.
    Gene; 2018 Sep 25; 672():64-71. PubMed ID: 29864494
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