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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

133 related articles for article (PubMed ID: 7516459)

  • 1. Genetic testing and counselling for congenital bilateral absence of the vas deferens.
    Meschede D; Horst J; Williams C; Williamson R
    Lancet; 1994 Jun; 343(8912):1566-7. PubMed ID: 7516459
    [No Abstract]   [Full Text] [Related]  

  • 2. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel missense mutation A1081P in the cystic fibrosis transmembrane conductance regulator (CFTR) gene identified in a Laotian patient with congenital bilateral absence of the vas deferens.
    Ngukam A; Jacquemont ML; Souville I; Viel M; Beldjord C; Hubert D; Hughes JN; Bienvenu T
    J Trop Pediatr; 2004 Aug; 50(4):239-40. PubMed ID: 15357566
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The incidence of cystic fibrosis gene mutations in patients with congenital bilateral absence of the vas deferens in Scotland.
    Donat R; McNeill AS; Fitzpatrick DR; Hargreave TB
    Br J Urol; 1997 Jan; 79(1):74-7. PubMed ID: 9043501
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Male infertility caused by bilateral agenesis of the vas deferens: a new clinical form of cystic fibrosis?].
    Durieu I; Bey-Omar F; Rollet J; Boggio D; Bellon G; Morel Y; Vital Durand D
    Rev Med Interne; 1997; 18(2):114-8. PubMed ID: 9092029
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Male infertility as the only presenting sign of cystic fibrosis when homozygous for the mild mutation R117H.
    Bienvenu T; Beldjord C; Adjiman M; Kaplan JC
    J Med Genet; 1993 Sep; 30(9):797. PubMed ID: 7692051
    [No Abstract]   [Full Text] [Related]  

  • 7. Mutations of the cystic fibrosis gene and congenital absence of the vas deferens.
    Patrizio P; Leonard DG
    Results Probl Cell Differ; 2000; 28():175-86. PubMed ID: 10626298
    [No Abstract]   [Full Text] [Related]  

  • 8. Infertility in men with cystic fibrosis.
    Sokol RZ
    Curr Opin Pulm Med; 2001 Nov; 7(6):421-6. PubMed ID: 11706320
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Congenital absence of the vas deferens: incomplete penetrance of cystic fibrosis gene mutations.
    Shin D; Gilbert F; Goldstein M; Schlegel PN
    J Urol; 1997 Nov; 158(5):1794-8; discussion 1798-9. PubMed ID: 9334604
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Genetically determined male infertility caused by the CFTR gene mutations].
    Sobczynska-Tomaszewska A
    Med Wieku Rozwoj; 2002; 6(4):335-47. PubMed ID: 12810986
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Compound heterozygosity for the delta F508 and F508C cystic fibrosis transmembrane conductance regulator (CFTR) mutations in a patient with congenital bilateral aplasia of the vas deferens.
    Meschede D; Eigel A; Horst J; Nieschlag E
    Am J Hum Genet; 1993 Jul; 53(1):292-3. PubMed ID: 7686336
    [No Abstract]   [Full Text] [Related]  

  • 15. Heterogeneous spectrum of mutations in CFTR gene from Indian patients with congenital absence of the vas deferens and their association with cystic fibrosis genetic modifiers.
    Sharma H; Mavuduru RS; Singh SK; Prasad R
    Mol Hum Reprod; 2014 Sep; 20(9):827-35. PubMed ID: 24958810
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 64(3):213-8. PubMed ID: 15239534
    [TBL] [Abstract][Full Text] [Related]  

  • 17. p.Leu636Pro mutation is associated with cystic fibrosis transmembrane conductance regulator-related disorders (congenital bilateral absence of vas deferens).
    Salvatore D; Dell'Edera D; Colangelo C; Smaldore G
    Int J Urol; 2015 Aug; 22(8):803-4. PubMed ID: 25944622
    [No Abstract]   [Full Text] [Related]  

  • 18. Editorial Comment to p.Leu636Pro mutation is associated with cystic fibrosis transmembrane conductance regulator-related disorders (congenital bilateral absence of vas deferens).
    Castaldo G; Amato F
    Int J Urol; 2015 Aug; 22(8):804. PubMed ID: 26010140
    [No Abstract]   [Full Text] [Related]  

  • 19. Cystic fibrosis patients, infertile men, and their noses.
    Pradal U; Piacentini GL
    Am J Respir Crit Care Med; 2004 Jan; 169(2):141-2. PubMed ID: 14718229
    [No Abstract]   [Full Text] [Related]  

  • 20. 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
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.