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Journal Abstract Search

344 related items for PubMed ID: 22340520

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  • 2. Association of cystic fibrosis transmembrane-conductance regulator gene mutation with negative outcome of intracytoplasmic sperm injection pregnancy in cases of congenital bilateral absence of vas deferens.
    Lu S, Cui Y, Li X, Zhang H, Liu J, Kong B, Cai F, Chen ZJ.
    Fertil Steril; 2014 May; 101(5):1255-60. PubMed ID: 24559724
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  • 4. 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 May; 29(1):35-40. PubMed ID: 17673436
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  • 6. 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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  • 7. 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; 39(1):76-9. PubMed ID: 22148899
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  • 8. 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; 9(2):588-598. PubMed ID: 33095972
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  • 9. 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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  • 10. 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 10; 21(4):826-836. PubMed ID: 30214069
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  • 13. 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 10; 16(4):292-6. PubMed ID: 22103471
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  • 15. Male partners of infertile couples with congenital unilateral absence of the vas deferens are mainly non-azoospermic.
    Mieusset R, Bieth E, Daudin M, Isus F, Delaunay B, Bujan L, Monteil L, Fauquet I, Huyghe E, Hamdi SM.
    Andrology; 2020 May 10; 8(3):645-653. PubMed ID: 31872980
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  • 16. Heterogeneity for mutations in the CFTR gene and clinical correlations in patients with congenital absence of the vas deferens.
    Casals T, Bassas L, Egozcue S, Ramos MD, Giménez J, Segura A, Garcia F, Carrera M, Larriba S, Sarquella J, Estivill X.
    Hum Reprod; 2000 Jul 10; 15(7):1476-83. PubMed ID: 10875853
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  • 17. 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 10; 24(5):1229-36. PubMed ID: 19181743
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  • 18. A rare frameshift variant in trans with the IVS9-5T allele of CFTR in a Chinese pedigree with congenital aplasia of vas deferens.
    Ge B, Zhang M, Wang R, Wang D, Li T, Li H, Wang B.
    J Assist Reprod Genet; 2019 Dec 10; 36(12):2541-2545. PubMed ID: 31709488
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  • 19. Mutations of the cystic fibrosis transmembrane conductance regulator gene in males with congenital bilateral absence of the vas deferens: Reproductive implications and genetic counseling (Review).
    Cui X, Wu X, Li Q, Jing X.
    Mol Med Rep; 2020 Nov 10; 22(5):3587-3596. PubMed ID: 33000223
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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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