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Journal Abstract Search

344 related items for PubMed ID: 22340520

  • 21.
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  • 22.
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  • 23. Novel mutations and polymorphisms in the CFTR gene associated with three subtypes of congenital absence of vas deferens.
    Yang X, Sun Q, Yuan P, Liang H, Wu X, Lai L, Zhang Y.
    Fertil Steril; 2015 Nov; 104(5):1268-75.e1-2. PubMed ID: 26277102
    [Abstract] [Full Text] [Related]

  • 24. 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 Nov; 11(6):480. PubMed ID: 10200050
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  • 25. 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; 90(5):2004.e23-6. PubMed ID: 18703181
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  • 26. CFTR mutations and polymorphisms in male infertility.
    Cuppens H, Cassiman JJ.
    Int J Androl; 2004 Oct; 27(5):251-6. PubMed ID: 15379964
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  • 27. Molecular analysis of the IVS8-T splice variant 5T and M470V exon 10 missense polymorphism in Iranian males with congenital bilateral absence of the vas deferens.
    Radpour R, Gilani MA, Gourabi H, Dizaj AV, Mollamohamadi S.
    Mol Hum Reprod; 2006 Jul; 12(7):469-73. PubMed ID: 16714368
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  • 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 Jul; 30(5):48-53. PubMed ID: 9026991
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  • 29. Genetics of the congenital absence of the vas deferens.
    Bieth E, Hamdi SM, Mieusset R.
    Hum Genet; 2021 Jan; 140(1):59-76. PubMed ID: 32025909
    [Abstract] [Full Text] [Related]

  • 30. The detection and significance of cystic fibrosis transmembrane conductance regulator gene promoter mutations in Chinese patients with congenital bilateral absence of the vas deferens.
    Bai S, Du Q, Liu X, Tong Y, Wu B.
    Gene; 2018 Sep 25; 672():64-71. PubMed ID: 29864494
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  • 31. A Survey of the Common Mutations and IVS8-Tn Polymorphism of Cystic Fibrosis Transmembrane Conductance Regulator Gene in Infertile Men with Nonobstructive Azoospermia and CBAVD in Iranian Population.
    Asadi F, Mirfakhraie R, Mirzajani F, Khedri A.
    Iran Biomed J; 2019 Mar 25; 23(2):92-8. PubMed ID: 29986553
    [Abstract] [Full Text] [Related]

  • 32. Identification of two mutations (S50Y and 4173delC) in the CFTR gene from patients with congenital bilateral absence of vas deferens (CBAVD).
    Zielenski J, Patrizio P, Markiewicz D, Asch RH, Tsui LC.
    Hum Mutat; 1997 Mar 25; 9(2):183-4. PubMed ID: 9067761
    [No Abstract] [Full Text] [Related]

  • 33. 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 25; 19(3):540-6. PubMed ID: 14998948
    [Abstract] [Full Text] [Related]

  • 34. Molecular study of (TG)m(T)n polymorphisms in Iranian males with congenital bilateral absence of the vas deferens.
    Radpour R, Gourabi H, Gilani MA, Dizaj AV.
    J Androl; 2007 Mar 25; 28(4):541-7. PubMed ID: 17314234
    [Abstract] [Full Text] [Related]

  • 35. 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 Mar 25; 29(5):506-13. PubMed ID: 18567645
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  • 36.
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  • 37. Different cystic fibrosis transmembrane conductance regulator mutations in Chinese men with congenital bilateral absence of vas deferens and other acquired obstructive azoospermia.
    Lu S, Yang X, Cui Y, Li X, Zhang H, Liu J, Chen ZJ.
    Urology; 2013 Oct 25; 82(4):824-8. PubMed ID: 23953609
    [Abstract] [Full Text] [Related]

  • 38. Cystic fibrosis transmembrane regulator mutation and congenital bilateral absence of the vas deferens: a bad combination for successful intracytoplasmic sperm injection outcomes.
    Ramasamy R, Lipshultz LI.
    Fertil Steril; 2014 May 25; 101(5):1246. PubMed ID: 24636394
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