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

PUBMED FOR HANDHELDS

Journal Abstract Search

215 related items for PubMed ID: 10081860

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23. Molecular diagnosis of congenital bilateral absence of the vas deferens: analyses of the CFTR gene in 64 French patients.
    Bienvenu T, Adjiman M, Thiounn N, Jeanpierre M, Hubert D, Lepercoq J, Francoual C, Wolf J, Izard V, Jouannet P, Kaplan JC, Beldjord C.
    Ann Genet; 1997; 40(1):5-9. PubMed ID: 9150843
    [Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25. 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
    [Abstract] [Full Text] [Related]

  • 26. A novel missense mutation P1290S at exon-20 of the CFTR gene in a Portuguese patient with congenital bilateral absence of the vas deferens.
    Grangeia A, Carvalho F, Fernandes S, Silva J, Sousa M, Barros A.
    Fertil Steril; 2005 Feb; 83(2):448-51. PubMed ID: 15705389
    [Abstract] [Full Text] [Related]

  • 27. Study of mutant and polyvariant mutant CFTR genes in patients with congenital absence of the vas deferens.
    Ravnik-Glavac M, Dean M, Glavac D.
    Pflugers Arch; 2000 Feb; 439(3 Suppl):R53-5. PubMed ID: 10653141
    [Abstract] [Full Text] [Related]

  • 28. [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 Feb; 30(5):48-53. PubMed ID: 9026991
    [Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30. [Cystic fibrosis transmembrane conductance regulator (CFTR) gene: mutations and clinical phenotypes].
    Schwartz M.
    Ugeskr Laeger; 2003 Feb 24; 165(9):912-6. PubMed ID: 12661515
    [Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32. Genetic findings in congenital bilateral aplasia of vas deferens patients and identification of six novel mutatations. Mutations in brief no. 138. Online.
    de Meeus A, Guittard C, Desgeorges M, Carles S, Demaille J, Claustres M.
    Hum Mutat; 1998 Feb 24; 11(6):480. PubMed ID: 10200050
    [Abstract] [Full Text] [Related]

  • 33. 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 Feb 24; 16(2):143-56. PubMed ID: 10923036
    [Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35. Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs.
    Stuppia L, Antonucci I, Binni F, Brandi A, Grifone N, Colosimo A, De Santo M, Gatta V, Gelli G, Guida V, Majore S, Calabrese G, Palka C, Ravani A, Rinaldi R, Tiboni GM, Ballone E, Venturoli A, Ferlini A, Torrente I, Grammatico P, Calzolari E, Dallapiccola B.
    Eur J Hum Genet; 2005 Aug 24; 13(8):959-64. PubMed ID: 15870824
    [Abstract] [Full Text] [Related]

  • 36. [Correlation of genitourinary abnormalities, spermiogram and CFTR genotype in patients with bilateral agenesis of the vas deferens].
    de la Taille A, Rigot JM, Mahe P, Gervais R, Dumur V, Lemaitre L, Mazeman E.
    Prog Urol; 1998 Jun 24; 8(3):370-6. PubMed ID: 9689669
    [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 24; 12(11):717-21. PubMed ID: 16973827
    [Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39. Improved detection of cystic fibrosis mutations in infertility patients with DNA sequence analysis.
    Danziger KL, Black LD, Keiles SB, Kammesheidt A, Turek PJ.
    Hum Reprod; 2004 Mar 24; 19(3):540-6. PubMed ID: 14998948
    [Abstract] [Full Text] [Related]

  • 40. 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 Mar 24; 53():261-70. PubMed ID: 10645285
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 11.