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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

187 related items for PubMed ID: 10702861

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  • 23. 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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  • 25. Detection of cystic fibrosis transmembrane conductance regulator (CFTR) gene rearrangements enriches the mutation spectrum in congenital bilateral absence of the vas deferens and impacts on genetic counselling.
    Ratbi I, Legendre M, Niel F, Martin J, Soufir JC, Izard V, Costes B, Costa C, Goossens M, Girodon E.
    Hum Reprod; 2007 May; 22(5):1285-91. PubMed ID: 17329263
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  • 28. Genetic investigations of CFTR mutations in congenital absence of vas deferens, uterus, and vagina as a cause of infertility.
    Radpour R, Gourabi H, Dizaj AV, Holzgreve W, Zhong XY.
    J Androl; 2008 May; 29(5):506-13. PubMed ID: 18567645
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  • 30. Congenital bilateral absence of vas deferens in the absence of cystic fibrosis.
    Augarten A, Yahav Y, Kerem BS, Halle D, Laufer J, Szeinberg A, Dor J, Mashiach S, Gazit E, Madgar I.
    Lancet; 1994 Nov 26; 344(8935):1473-4. PubMed ID: 7968122
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  • 31. Agenesis or atrophy of the testis and vas deferens.
    Mercer S.
    Can J Surg; 1979 May 26; 22(3):245-6. PubMed ID: 35276
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  • 33. Contribution of investigations to the diagnosis of bilateral vas aplasia.
    Kumar R, Thulkar S, Kumar V, Jagannathan NR, Gupta NP.
    ANZ J Surg; 2005 Sep 26; 75(9):807-9. PubMed ID: 16173998
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  • 39. 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 26; 90(5):2004.e23-6. PubMed ID: 18703181
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