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Journal Abstract Search

447 related items for PubMed ID: 27488005

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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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  • 5. 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 Sep 10; 29(1):35-40. PubMed ID: 17673436
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  • 7. [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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  • 9. 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 18; 19(11):2502-8. PubMed ID: 15333598
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  • 11. 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 18; 118(12):1576-1583. PubMed ID: 30797621
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  • 12. 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 18; 23(2):92-8. PubMed ID: 29986553
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  • 14. Cystic fibrosis transmembrane conductance regulator-related male infertility: Relevance of genetic testing & counselling in Indian population.
    Gaikwad A, Khan S, Kadam S, Shah R, Kulkarni V, Kumaraswamy R, Kadam K, Dighe V, Gajbhiye R.
    Indian J Med Res; 2020 Dec 18; 152(6):575-583. PubMed ID: 34145097
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  • 17. 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 18; 21(4):826-836. PubMed ID: 30214069
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  • 18. 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 18; 74(6):1164-74. PubMed ID: 11119745
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  • 19. Screening of ΔF508 mutation and IVS8-poly T polymorphism in CFTR gene in Tunisian infertile men without CBAVD.
    Ghorbel M, Baklouti-Gargouri S, Keskes R, Sellami-Ben Hamida A, Feki-Chakroun N, Bahloul A, Fakhfakh F, Ammar-Keskes L.
    Andrologia; 2012 May 18; 44 Suppl 1():376-82. PubMed ID: 21762191
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  • 20. 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 18; 16(4):292-6. PubMed ID: 22103471
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