These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

152 related articles for article (PubMed ID: 23214250)

  • 21. 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; 23(2):92-8. PubMed ID: 29986553
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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; 82(4):824-8. PubMed ID: 23953609
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Analysis of CNVs of CFTR gene in Chinese Han population with CBAVD.
    Ma C; Wang R; Li T; Li H; Wang B
    Mol Genet Genomic Med; 2020 Nov; 8(11):e1506. PubMed ID: 32951344
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Prevalence of CBAVD in azoospermic men carrying pathogenic CFTR mutations - Evaluated in a cohort of 639 non-vasectomized azoospermic men.
    Fedder J; Jørgensen MW; Engvad B
    Andrology; 2021 Mar; 9(2):588-598. PubMed ID: 33095972
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Mutations in the cystic fibrosis gene in men with congenital bilateral absence of the vas deferens.
    De Braekeleer M; Férec C
    Mol Hum Reprod; 1996 Sep; 2(9):669-77. PubMed ID: 9239681
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Congenital bilateral absence of the vas deferens: clinical characteristics, biological parameters, cystic fibrosis transmembrane conductance regulator gene mutations, and implications for genetic counseling.
    Daudin M; Bieth E; Bujan L; Massat G; Pontonnier F; Mieusset R
    Fertil Steril; 2000 Dec; 74(6):1164-74. PubMed ID: 11119745
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Diagnostics of CFTR-negative patients with congenital bilateral absence of vas deferens: which mutations are of most interest?
    Ferlin A; Stuppia L
    Expert Rev Mol Diagn; 2020 Mar; 20(3):265-267. PubMed ID: 31854215
    [No Abstract]   [Full Text] [Related]  

  • 29. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Mutations of the cystic fibrosis transmembrane conductance regulator gene in males with congenital bilateral absence of the vas deferens: Reproductive implications and genetic counseling (Review).
    Cui X; Wu X; Li Q; Jing X
    Mol Med Rep; 2020 Nov; 22(5):3587-3596. PubMed ID: 33000223
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Correlation between CFTR 5T polymorphisms and the risk of congenital bilateral absence of the vas deferens].
    Zhao GG; Sun HB; Zhi HJ; Wang F; Wu QY; Xia XY; Xu XF
    Zhonghua Nan Ke Xue; 2019 Mar; 25(3):231-237. PubMed ID: 32216241
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Cystic fibrosis transmembrane conductance regulator gene mutations in infertile males with congenital bilateral absence of the vas deferens.
    Uzun S; Gökçe S; Wagner K
    Tohoku J Exp Med; 2005 Dec; 207(4):279-85. PubMed ID: 16272798
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Significance of CFTR gene mutations in patients with congenital aplasia of vas deferens with special regard to renal aplasia.
    Schwarzer JU; Schwarz M
    Andrologia; 2012 Oct; 44(5):305-7. PubMed ID: 22340520
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Mutation studies in the CFTR gene in Asian Indian subjects with congenital bilateral absence of vas deferens: report of two novel mutations and four novel variants.
    Sachdeva K; Saxena R; Majumdar A; Chadha S; Verma IC
    Genet Test Mol Biomarkers; 2011 May; 15(5):307-12. PubMed ID: 21254931
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Compound heterozygous mutations in CFTR causing CBAVD in Chinese pedigrees.
    Yang B; Wang X; Zhang W; Li H; Wang B
    Mol Genet Genomic Med; 2018 Nov; 6(6):1097-1103. PubMed ID: 30450785
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Correlation between CFTR gene mutations in Iranian men with congenital absence of the vas deferens and anatomical genital phenotype.
    Radpour R; Gourabi H; Gilani MA; Dizaj AV
    J Androl; 2008; 29(1):35-40. PubMed ID: 17673436
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [Detection of CFTR gene mutations in azoospermia patients with congenital unilateral absence of the vas deferens].
    Yang XJ; Yuan P; Wu X; Zhang H; He QQ; Zhang Y
    Zhonghua Nan Ke Xue; 2015 Mar; 21(3):229-33. PubMed ID: 25898554
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Increased frequency of CFTR gene mutations identified in Indian infertile men with non-CBAVD obstructive azoospermia and spermatogenic failure.
    Sharma H; Mavuduru RS; Singh SK; Prasad R
    Gene; 2014 Sep; 548(1):43-7. PubMed ID: 25010724
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens.
    Chillón M; Casals T; Mercier B; Bassas L; Lissens W; Silber S; Romey MC; Ruiz-Romero J; Verlingue C; Claustres M
    N Engl J Med; 1995 Jun; 332(22):1475-80. PubMed ID: 7739684
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.