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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

447 related items for PubMed ID: 27488005

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  • 25. Cystic fibrosis transmembrane conductance regulator mutations and polymorphisms associated with congenital bilateral absence of vas deferens in a restricted group of patients from North Africa.
    Boudaya M, Fredj SH, Haj RB, Khrouf M, Bouker A, Halouani L, Messaoud T.
    Ann Hum Biol; 2012 Jan; 39(1):76-9. PubMed ID: 22148899
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  • 27. 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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  • 28. Congenital bilateral absence of the vas deferens as an atypical form of cystic fibrosis: reproductive implications and genetic counseling.
    de Souza DAS, Faucz FR, Pereira-Ferrari L, Sotomaior VS, Raskin S.
    Andrology; 2018 Jan; 6(1):127-135. PubMed ID: 29216686
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  • 30. Extensive analysis of 40 infertile patients with congenital absence of the vas deferens: in 50% of cases only one CFTR allele could be detected.
    Casals T, Bassas L, Ruiz-Romero J, Chillón M, Giménez J, Ramos MD, Tapia G, Narváez H, Nunes V, Estivill X.
    Hum Genet; 1995 Feb; 95(2):205-11. PubMed ID: 7532150
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  • 34. Genetic diagnosis and sperm retrieval outcomes for Chinese patients with congenital bilateral absence of vas deferens.
    Wang H, An M, Liu Y, Hu K, Jin Y, Xu S, Chen B, Lu M.
    Andrology; 2020 Sep; 8(5):1064-1069. PubMed ID: 32020786
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