These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


608 related items for PubMed ID: 12660625

  • 1. Congenital absence of vas deferens and cystic fibrosis.
    Leonardi S, Bombace V, Rotolo N, Sciuto C, La Rosa M.
    Minerva Pediatr; 2003 Feb; 55(1):43-7, 47-50. PubMed ID: 12660625
    [Abstract] [Full Text] [Related]

  • 2. Mutations in CFTR gene and clinical correlation in Argentine patients with congenital bilateral absence of the vas deferens.
    Levy EM, Granados P, Rawe V, Olmedo SB, Luna MC, Cafferata E, Pivetta OH.
    Medicina (B Aires); 2004 Feb; 64(3):213-8. PubMed ID: 15239534
    [Abstract] [Full Text] [Related]

  • 3. 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 Feb; 29(1):35-40. PubMed ID: 17673436
    [Abstract] [Full Text] [Related]

  • 4. Mutations of the CFTR gene in Turkish patients with congenital bilateral absence of the vas deferens.
    Dayangaç D, Erdem H, Yilmaz E, Sahin A, Sohn C, Ozgüç M, Dörk T.
    Hum Reprod; 2004 May; 19(5):1094-100. PubMed ID: 15070876
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutation associated with a congenital bilateral absence of vas deferens.
    Sakamoto H, Yajima T, Suzuki K, Ogawa Y.
    Int J Urol; 2008 Mar; 15(3):270-1. PubMed ID: 18304229
    [Abstract] [Full Text] [Related]

  • 8. 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]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. 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]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. 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; 24(5):1229-36. PubMed ID: 19181743
    [Abstract] [Full Text] [Related]

  • 19. CFTR mutations and polymorphisms in male infertility.
    Cuppens H, Cassiman JJ.
    Int J Androl; 2004 Oct; 27(5):251-6. PubMed ID: 15379964
    [Abstract] [Full Text] [Related]

  • 20. Urogenital anomalies in men with congenital absence of the vas deferens.
    Schlegel PN, Shin D, Goldstein M.
    J Urol; 1996 May; 155(5):1644-8. PubMed ID: 8627844
    [Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 31.