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Journal Abstract Search

321 related items for PubMed ID: 9675940

  • 21.
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  • 24. Assisted reproduction technology for patients with congenital bilateral absence of vas deferens.
    Okada H, Yoshimura K, Fujioka H, Tatsumi N, Gotoh A, Fujisawa M, Gohji K, Arakawa S, Kato H, Kobayashi SI, Isojima S, Koshida M, Kamidono S.
    J Urol; 1999 Apr; 161(4):1157-62. PubMed ID: 10081860
    [Abstract] [Full Text] [Related]

  • 25. [Congenital agenesis of the vas deferens and cystic fibrosis].
    Kugler A, Laccone F, Weidner W, Kallerhoff M.
    Urologe A; 1995 Jul; 34(4):348-50. PubMed ID: 7545847
    [Abstract] [Full Text] [Related]

  • 26. Cystic fibrosis as a cause of infertility.
    Jarzabek K, Zbucka M, Pepiński W, Szamatowicz J, Domitrz J, Janica J, Wołczyński S, Szamatowicz M.
    Reprod Biol; 2004 Jul; 4(2):119-29. PubMed ID: 15297887
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  • 28. Expression of the cystic fibrosis transmembrane conductance regulator (CFTR) mRNA in normal and pathological adult human epididymis.
    Patrizio P, Salameh WA.
    J Reprod Fertil Suppl; 1998 Jul; 53():261-70. PubMed ID: 10645285
    [Abstract] [Full Text] [Related]

  • 29. Genetics of cystic fibrosis.
    Lommatzsch ST, Aris R.
    Semin Respir Crit Care Med; 2009 Oct; 30(5):531-8. PubMed ID: 19760540
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  • 30. Detection of cystic fibrosis transmembrane conductance regulator (CFTR) gene rearrangements enriches the mutation spectrum in congenital bilateral absence of the vas deferens and impacts on genetic counselling.
    Ratbi I, Legendre M, Niel F, Martin J, Soufir JC, Izard V, Costes B, Costa C, Goossens M, Girodon E.
    Hum Reprod; 2007 May; 22(5):1285-91. PubMed ID: 17329263
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  • 31. The role of the F508C mutation in congenital bilateral absence of the vas deferens.
    Havasi V, Keiles S, Hambuch T, Sorscher EJ, Kammesheidt A.
    Genet Med; 2008 Dec; 10(12):910-4. PubMed ID: 19092444
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  • 32.
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  • 33. Genetic investigations of CFTR mutations in congenital absence of vas deferens, uterus, and vagina as a cause of infertility.
    Radpour R, Gourabi H, Dizaj AV, Holzgreve W, Zhong XY.
    J Androl; 2008 Dec; 29(5):506-13. PubMed ID: 18567645
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  • 34. [An analysis of the mutations in the gene of the mucoviscidosis transmembrane regulator protein (MTRP) in patients with congenital bilateral aplasia of the vas deferens].
    Gusak NM, Gorovenko NG, Gorpinchenko II, Karmeliuk SO.
    Tsitol Genet; 1996 Dec; 30(5):48-53. PubMed ID: 9026991
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  • 36. 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; 12(7):469-73. PubMed ID: 16714368
    [Abstract] [Full Text] [Related]

  • 37. 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; 12(11):717-21. PubMed ID: 16973827
    [Abstract] [Full Text] [Related]

  • 38. CFTR mutations and polymorphisms in male infertility.
    Cuppens H, Cassiman JJ.
    Int J Androl; 2004 Oct; 27(5):251-6. PubMed ID: 15379964
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  • 39. Analysis of the CFTR gene in Iranian cystic fibrosis patients: identification of eight novel mutations.
    Alibakhshi R, Kianishirazi R, Cassiman JJ, Zamani M, Cuppens H.
    J Cyst Fibros; 2008 Mar; 7(2):102-9. PubMed ID: 17662673
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  • 40. Vas deferens anomalies in paediatric age.
    Campagnola S, Fasoli L, Flessati P, Sulpasso M, Castellani C.
    Minerva Pediatr; 1999 Mar; 51(7-8):265-9. PubMed ID: 10634059
    [Abstract] [Full Text] [Related]

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