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Journal Abstract Search

264 related items for PubMed ID: 10200050

  • 1. 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; 11(6):480. PubMed ID: 10200050
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  • 5. 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
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  • 6. 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
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  • 7. Characterization of cystic fibrosis conductance transmembrane regulator gene mutations and IVS8 poly(T) variants in Portuguese patients with congenital absence of the vas deferens.
    Grangeia A, Niel F, Carvalho F, Fernandes S, Ardalan A, Girodon E, Silva J, Ferrás L, Sousa M, Barros A.
    Hum Reprod; 2004 Nov; 19(11):2502-8. PubMed ID: 15333598
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  • 10. 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 Nov; 64(3):213-8. PubMed ID: 15239534
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  • 12. A novel missense mutation D513G in exon 10 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene identified in a French CBAVD patient. Mutations in brief no. 175. Online.
    Bienvenu T, Bousquet S, Vidaud D, Hubert D, Francoual C, Beldjord C, Kaplan JC.
    Hum Mutat; 1998 Nov; 12(3):213-4. PubMed ID: 10651488
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  • 13. 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
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  • 14. 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 Nov; 439(3 Suppl):R53-5. PubMed ID: 10653141
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  • 15. [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 Nov; 30(5):48-53. PubMed ID: 9026991
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  • 17. 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
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