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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

185 related items for PubMed ID: 10651488

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  • 4. 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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  • 8. 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
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  • 17. 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 May; 439(3 Suppl):R53-5. PubMed ID: 10653141
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  • 19. Association of cystic fibrosis transmembrane-conductance regulator gene mutation with negative outcome of intracytoplasmic sperm injection pregnancy in cases of congenital bilateral absence of vas deferens.
    Lu S, Cui Y, Li X, Zhang H, Liu J, Kong B, Cai F, Chen ZJ.
    Fertil Steril; 2014 May; 101(5):1255-60. PubMed ID: 24559724
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  • 20. [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 May; 30(5):48-53. PubMed ID: 9026991
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