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 *

305 related articles for article (PubMed ID: 30450785)

  • 21. Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) in Chinese patients with congenital bilateral absence of vas deferens.
    Li H; Wen Q; Li H; Zhao L; Zhang X; Wang J; Cheng L; Yang J; Chen S; Ma X; Wang B
    J Cyst Fibros; 2012 Jul; 11(4):316-23. PubMed ID: 22483971
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Homozygous 5T alleles, clinical presentation and genetic analysis within a family with congenital bilateral absence of the vas deferens].
    Feng JR; Zhang YN; Wu X; Yang XJ; Chen ST; Ma GC; Luo SG; Zhang Y
    Zhonghua Yi Xue Za Zhi; 2018 May; 98(18):1414-1418. PubMed ID: 29804404
    [No Abstract]   [Full Text] [Related]  

  • 23. Molecular screening of the CFTR gene in Mexican patients with congenital absence of the vas deferens.
    Saldaña-Alvarez Y; Jiménez-Morales S; Echevarría-Sánchez M; Jiménez-Ruíz JL; García-Cavazos R; Velázquez-Cruz R; Carnevale A; Orozco L
    Genet Test Mol Biomarkers; 2012 Apr; 16(4):292-6. PubMed ID: 22103471
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The CFTR gene mild variants poly-T, TG repeats and M470V detection in Indian men with congenital bilateral absence of vas deferens.
    Gaikwad A; Khan S; Kadam S; Kadam K; Dighe V; Shah R; Kulkarni V; Kumaraswamy R; Gajbhiye R
    Andrologia; 2018 Mar; 50(2):. PubMed ID: 28776713
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. 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]  

  • 27. 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]  

  • 28. [Detection of the mutation of all the exons of the CFTR gene in Chinese men with congenital bilateral absence of the vas deferens].
    Du Q; Fang YY; Pan YF; Pan BC; Song YS; Wu B
    Zhonghua Nan Ke Xue; 2012 Nov; 18(11):999-1003. PubMed ID: 23214250
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Heterogeneous spectrum of mutations in CFTR gene from Indian patients with congenital absence of the vas deferens and their association with cystic fibrosis genetic modifiers.
    Sharma H; Mavuduru RS; Singh SK; Prasad R
    Mol Hum Reprod; 2014 Sep; 20(9):827-35. PubMed ID: 24958810
    [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. 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]  

  • 32. [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]  

  • 33. 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]  

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

  • 35. [Association of CFTR gene polymorphism with congenital bilateral absence of vas deferens in ethnic Han Chinese patients].
    Liu LJ; Li HG; Gu X; Zhu JW; Zhao K; Tang YP; Xiong CL
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Dec; 30(6):729-32. PubMed ID: 24327157
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Improved detection of CFTR variants by targeted next-generation sequencing in male infertility: a case series.
    Smits RM; Oud MS; Vissers LELM; Lugtenberg D; Braat DDM; Fleischer K; Ramos L; D'Hauwers KWM
    Reprod Biomed Online; 2019 Dec; 39(6):963-968. PubMed ID: 31672438
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Common CFTR haplotypes and susceptibility to chronic pancreatitis and congenital bilateral absence of the vas deferens.
    Steiner B; Rosendahl J; Witt H; Teich N; Keim V; Schulz HU; Pfützer R; Löhr M; Gress TM; Nickel R; Landt O; Koudova M; Macek M; Farre A; Casals T; Desax MC; Gallati S; Gomez-Lira M; Audrezet MP; Férec C; des Georges M; Claustres M; Truninger K
    Hum Mutat; 2011 Aug; 32(8):912-20. PubMed ID: 21520337
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Enhanced frequency of CFTR gene variants in couples who are candidates for assisted reproductive technology treatment.
    Tomaiuolo R; Fausto M; Elce A; Strina I; Ranieri A; Amato F; Castaldo G; De Placido G; Alviggi C
    Clin Chem Lab Med; 2011 Aug; 49(8):1289-1293. PubMed ID: 21679131
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 16.