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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

312 related items for PubMed ID: 32025909

  • 1. 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]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Novel ADGRG2 truncating variants in patients with X-linked congenital absence of vas deferens.
    Pagin A, Bergougnoux A, Girodon E, Reboul MP, Willoquaux C, Kesteloot M, Raynal C, Bienvenu T, Humbert M, Lalau G, Bieth E.
    Andrology; 2020 May; 8(3):618-624. PubMed ID: 31845523
    [Abstract] [Full Text] [Related]

  • 4. Truncating Mutations in the Adhesion G Protein-Coupled Receptor G2 Gene ADGRG2 Cause an X-Linked Congenital Bilateral Absence of Vas Deferens.
    Patat O, Pagin A, Siegfried A, Mitchell V, Chassaing N, Faguer S, Monteil L, Gaston V, Bujan L, Courtade-Saïdi M, Marcelli F, Lalau G, Rigot JM, Mieusset R, Bieth E.
    Am J Hum Genet; 2016 Aug 04; 99(2):437-42. PubMed ID: 27476656
    [Abstract] [Full Text] [Related]

  • 5. Expanding the phenotypic and genetic spectrum of Chinese patients with congenital absence of vas deferens bearing CFTR and ADGRG2 alleles.
    Yuan P, Liang ZK, Liang H, Zheng LY, Li D, Li J, Zhang J, Tian J, Lai LH, Zhang K, He ZY, Zhang QX, Wang WJ.
    Andrology; 2019 May 04; 7(3):329-340. PubMed ID: 30811104
    [Abstract] [Full Text] [Related]

  • 6. Association of cystic fibrosis transmembrane-conductance regulator gene mutation with negative outcome of intracytoplasmic sperm injection pregnancy in cases of congenital bilateral absence of vas deferens.
    Lu S, Cui Y, Li X, Zhang H, Liu J, Kong B, Cai F, Chen ZJ.
    Fertil Steril; 2014 May 04; 101(5):1255-60. PubMed ID: 24559724
    [Abstract] [Full Text] [Related]

  • 7. A novel hemizygous loss-of-function mutation in ADGRG2 causes male infertility with congenital bilateral absence of the vas deferens.
    Wu H, Gao Y, Ma C, Shen Q, Wang J, Lv M, Liu C, Cheng H, Zhu F, Tian S, Elshewy N, Ni X, Tan Q, Xu X, Zhou P, Wei Z, Zhang F, He X, Cao Y.
    J Assist Reprod Genet; 2020 Jun 04; 37(6):1421-1429. PubMed ID: 32314195
    [Abstract] [Full Text] [Related]

  • 8. [Detection of pathogenic gene mutations in thirteen cases of congenital bilateral absence of vas deferens infertility patients].
    Tang Y, Zhang Y, Wu D, Lin Y, Lan F.
    Beijing Da Xue Xue Bao Yi Xue Ban; 2024 Oct 18; 56(5):763-774. PubMed ID: 39397452
    [Abstract] [Full Text] [Related]

  • 9. 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 18; 20(9):827-35. PubMed ID: 24958810
    [Abstract] [Full Text] [Related]

  • 10. 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 18; 44(5):305-7. PubMed ID: 22340520
    [Abstract] [Full Text] [Related]

  • 11. 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 18; 9(2):588-598. PubMed ID: 33095972
    [Abstract] [Full Text] [Related]

  • 12. Genetic mutation analysis of 22 patients with congenital absence of vas deferens: a single-center study†.
    Tan MQ, Huang WJ, Lan FH, Xu YJ, Zheng MY, Tang Y.
    Biol Reprod; 2022 Jan 13; 106(1):108-117. PubMed ID: 34673937
    [Abstract] [Full Text] [Related]

  • 13. 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 13; 6(1):127-135. PubMed ID: 29216686
    [Abstract] [Full Text] [Related]

  • 14. 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 13; 22(5):3587-3596. PubMed ID: 33000223
    [Abstract] [Full Text] [Related]

  • 15. Male partners of infertile couples with congenital unilateral absence of the vas deferens are mainly non-azoospermic.
    Mieusset R, Bieth E, Daudin M, Isus F, Delaunay B, Bujan L, Monteil L, Fauquet I, Huyghe E, Hamdi SM.
    Andrology; 2020 May 13; 8(3):645-653. PubMed ID: 31872980
    [Abstract] [Full Text] [Related]

  • 16. 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 13; 6(6):1097-1103. PubMed ID: 30450785
    [Abstract] [Full Text] [Related]

  • 17. Genetic analysis and intracytoplasmic sperm injection outcomes of Chinese patients with congenital bilateral absence of vas deferens.
    Cheng H, Yang S, Meng Q, Zheng B, Gu Y, Wang L, Song T, Xu C, Wang G, Han M, Shen L, Ding J, Li H, Ouyang J.
    J Assist Reprod Genet; 2022 Mar 13; 39(3):719-728. PubMed ID: 35119551
    [Abstract] [Full Text] [Related]

  • 18. 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 13; 23(2):92-8. PubMed ID: 29986553
    [Abstract] [Full Text] [Related]

  • 19. 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 10; 548(1):43-7. PubMed ID: 25010724
    [Abstract] [Full Text] [Related]

  • 20. A rare frameshift variant in trans with the IVS9-5T allele of CFTR in a Chinese pedigree with congenital aplasia of vas deferens.
    Ge B, Zhang M, Wang R, Wang D, Li T, Li H, Wang B.
    J Assist Reprod Genet; 2019 Dec 10; 36(12):2541-2545. PubMed ID: 31709488
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 16.