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Journal Abstract Search

234 related items for PubMed ID: 7539210

  • 1. CFTR haplotype analysis reveals genetic heterogeneity in the etiology of congenital bilateral aplasia of the vas deferens.
    Rave-Harel N, Madgar I, Goshen R, Nissim-Rafinia M, Ziadni A, Rahat A, Chiba O, Kalman YM, Brautbar C, Levinson D.
    Am J Hum Genet; 1995 Jun; 56(6):1359-66. PubMed ID: 7539210
    [Abstract] [Full Text] [Related]

  • 2. Is congenital bilateral absence of vas deferens a primary form of cystic fibrosis? Analyses of the CFTR gene in 67 patients.
    Mercier B, Verlingue C, Lissens W, Silber SJ, Novelli G, Bonduelle M, Audrézet MP, Férec C.
    Am J Hum Genet; 1995 Jan; 56(1):272-7. PubMed ID: 7529962
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  • 3. 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; 2(9):669-77. PubMed ID: 9239681
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  • 4. Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens.
    Chillón M, Casals T, Mercier B, Bassas L, Lissens W, Silber S, Romey MC, Ruiz-Romero J, Verlingue C, Claustres M.
    N Engl J Med; 1995 Jun 01; 332(22):1475-80. PubMed ID: 7739684
    [Abstract] [Full Text] [Related]

  • 5. Extensive analysis of 40 infertile patients with congenital absence of the vas deferens: in 50% of cases only one CFTR allele could be detected.
    Casals T, Bassas L, Ruiz-Romero J, Chillón M, Giménez J, Ramos MD, Tapia G, Narváez H, Nunes V, Estivill X.
    Hum Genet; 1995 Feb 01; 95(2):205-11. PubMed ID: 7532150
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  • 7. [Congenital agenesis of the vas deferens and cystic fibrosis].
    Kugler A, Laccone F, Weidner W, Kallerhoff M.
    Urologe A; 1995 Jul 01; 34(4):348-50. PubMed ID: 7545847
    [Abstract] [Full Text] [Related]

  • 8. 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 01; 143(5):616-23. PubMed ID: 27488005
    [Abstract] [Full Text] [Related]

  • 9. Molecular pathology of the CFTR locus in male infertility.
    Claustres M.
    Reprod Biomed Online; 2005 Jan 01; 10(1):14-41. PubMed ID: 15705292
    [Abstract] [Full Text] [Related]

  • 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 01; 12(7):469-73. PubMed ID: 16714368
    [Abstract] [Full Text] [Related]

  • 11. CFTR mutations and polymorphisms in male infertility.
    Cuppens H, Cassiman JJ.
    Int J Androl; 2004 Oct 01; 27(5):251-6. PubMed ID: 15379964
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  • 13. Identification of the second CFTR mutation in patients with congenital bilateral absence of vas deferens undergoing ART protocols.
    Giuliani R, Antonucci I, Torrente I, Grammatico P, Palka G, Stuppia L.
    Asian J Androl; 2010 Nov 01; 12(6):819-26. PubMed ID: 20657600
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  • 15. Congenital bilateral absence of the vas deferens as an atypical form of cystic fibrosis: reproductive implications and genetic counseling.
    de Souza DAS, Faucz FR, Pereira-Ferrari L, Sotomaior VS, Raskin S.
    Andrology; 2018 Jan 01; 6(1):127-135. PubMed ID: 29216686
    [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
    [Abstract] [Full Text] [Related]

  • 17. Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France.
    Claustres M, Guittard C, Bozon D, Chevalier F, Verlingue C, Ferec C, Girodon E, Cazeneuve C, Bienvenu T, Lalau G, Dumur V, Feldmann D, Bieth E, Blayau M, Clavel C, Creveaux I, Malinge MC, Monnier N, Malzac P, Mittre H, Chomel JC, Bonnefont JP, Iron A, Chery M, Georges MD.
    Hum Mutat; 2000 Oct 18; 16(2):143-56. PubMed ID: 10923036
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  • 18. [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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  • 19. Analysis of the whole CFTR coding regions and splice junctions in azoospermic men with congenital bilateral aplasia of epididymis or vas deferens.
    Culard JF, Desgeorges M, Costa P, Laussel M, Razakatzara G, Navratil H, Demaille J, Claustres M.
    Hum Genet; 1994 Apr 18; 93(4):467-70. PubMed ID: 7513294
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  • 20. 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 18; 20(9):2470-5. PubMed ID: 15905293
    [Abstract] [Full Text] [Related]

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