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 *

130 related articles for article (PubMed ID: 8188533)

  • 1. The genetic basis of congenital bilateral absence of the vas deferens and cystic fibrosis.
    Oates RD; Amos JA
    J Androl; 1994; 15(1):1-8. PubMed ID: 8188533
    [No Abstract]   [Full Text] [Related]  

  • 2. 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]  

  • 3. [Agenesis of vas deferens and cystic fibrosis].
    Calleja Escudero J; Telleria Orriols JJ; Estébanez Zarranz J; Alonso Ramos MJ; Amón Sesmero JH; Martínez-Sagarra JM; Blanco Quirós A
    Actas Urol Esp; 1997 Sep; 21(8):773-6. PubMed ID: 9412228
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Congenital bilateral agenesis of the vas deferens associated with cystic fibrosis. A molecular genetic study].
    Guzmán Martínez-Valls PL; Tomas Ros M; Glover López G; Ferrero Doria R; Morga Egea JP; Navas Pastor J; Rico Galiano JL; Sempere Gutiérrez A; Fontana Compiano LO
    Arch Esp Urol; 1998 Jun; 51(5):451-5. PubMed ID: 9675940
    [TBL] [Abstract][Full Text] [Related]  

  • 5. High frequency of the R117H cystic fibrosis mutation in patients with congenital absence of the vas deferens.
    Gervais R; Dumur V; Rigot JM; Lafitte JJ; Roussel P; Claustres M; Demaille J
    N Engl J Med; 1993 Feb; 328(6):446-7. PubMed ID: 8421472
    [No Abstract]   [Full Text] [Related]  

  • 6. Normal vas deferens in fetuses with cystic fibrosis.
    Gaillard DA; Carré-Pigeon F; Lallemand A
    J Urol; 1997 Oct; 158(4):1549-52. PubMed ID: 9302172
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Molecular basis of cystic fibrosis and congenital bilateral agenesis of vas deferens].
    Bienvenu T; Claustres M
    Contracept Fertil Sex; 1996 Jun; 24(6):495-500. PubMed ID: 8766513
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Identification of two mutations (S50Y and 4173delC) in the CFTR gene from patients with congenital bilateral absence of vas deferens (CBAVD).
    Zielenski J; Patrizio P; Markiewicz D; Asch RH; Tsui LC
    Hum Mutat; 1997; 9(2):183-4. PubMed ID: 9067761
    [No Abstract]   [Full Text] [Related]  

  • 9. Congenital bilateral absence of the vas deferens.
    Escobar MA; Lau ST; Glick PL
    J Pediatr Surg; 2008 Jun; 43(6):1222-3. PubMed ID: 18558214
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Molecular screening of CFTR gene in Brazilian men with bilateral agenesis of the vas deferens.
    Bertuzzo CS; Pinto W
    Hum Fertil (Camb); 2006 Mar; 9(1):53-6. PubMed ID: 16581722
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cystic fibrosis and congenital absence of the vas deferens.
    Rigot JM; Lafitte JJ; Dumur V; Gervais R; Manouvrier S; Biserte J; Mazeman E; Roussel P
    N Engl J Med; 1991 Jul; 325(1):64-5. PubMed ID: 2046716
    [No Abstract]   [Full Text] [Related]  

  • 12. Genetic diseases of the seminal ducts.
    Meschede D; Dworniczak B; Nieschlag E; Horst J
    Biomed Pharmacother; 1998; 52(5):197-203. PubMed ID: 9755815
    [TBL] [Abstract][Full Text] [Related]  

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

  • 14. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Outcome of intracytoplasmic sperm injection for a couple in which the man is carrier of CFTR p.[R74W;V201M;D1270N] and p.P841R mutations and his spouse a heterozygous carrier of p.F508del mutation of the cystic fibrosis transmembrane conductance regulator gene.
    Brugnon F; Bilan F; Heraud MC; Grizard G; Janny L; Creveaux I
    Fertil Steril; 2008 Nov; 90(5):2004.e23-6. PubMed ID: 18703181
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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
    [TBL] [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; 16(2):143-56. PubMed ID: 10923036
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Congenital bilateral absence of the vas deferens and cystic fibrosis.
    Lancet; 1992 May; 339(8805):1328-9. PubMed ID: 1349997
    [No Abstract]   [Full Text] [Related]  

  • 19. Congenital bilateral absence of the vas deferens and cryptorchidism without cystic fibrosis.
    Kim JH; Cromie WJ
    J Urol; 1996 Jun; 155(6):2060. PubMed ID: 8618335
    [No Abstract]   [Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.