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.
250 related articles for article (PubMed ID: 34145097)
1. Cystic fibrosis transmembrane conductance regulator-related male infertility: Relevance of genetic testing & counselling in Indian population. Gaikwad A; Khan S; Kadam S; Shah R; Kulkarni V; Kumaraswamy R; Kadam K; Dighe V; Gajbhiye R Indian J Med Res; 2020 Dec; 152(6):575-583. PubMed ID: 34145097 [TBL] [Abstract][Full Text] [Related]
2. Cystic fibrosis transmembrane conductance regulator (CFTR) gene abnormalities in Indian males with congenital bilateral absence of vas deferens & renal anomalies. Gajbhiye R; Kadam K; Khole A; Gaikwad A; Kadam S; Shah R; Kumaraswamy R; Khole V Indian J Med Res; 2016 May; 143(5):616-23. PubMed ID: 27488005 [TBL] [Abstract][Full Text] [Related]
3. [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; 56(5):763-774. PubMed ID: 39397452 [TBL] [Abstract][Full Text] [Related]
4. 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; 101(5):1255-60. PubMed ID: 24559724 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. CFTR mutations and polymorphisms in male infertility. Cuppens H; Cassiman JJ Int J Androl; 2004 Oct; 27(5):251-6. PubMed ID: 15379964 [TBL] [Abstract][Full Text] [Related]
8. 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 [TBL] [Abstract][Full Text] [Related]
9. Cystic fibrosis and infertility caused by congenital bilateral absence of the vas deferens and related clinical entities. Lissens W; Mercier B; Tournaye H; Bonduelle M; Férec C; Seneca S; Devroey P; Silber S; Van Steirteghem A; Liebaers I Hum Reprod; 1996 Dec; 11 Suppl 4():55-78; discussion 79-80. PubMed ID: 9147111 [TBL] [Abstract][Full Text] [Related]
10. 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]
11. Compound heterozygous mutations in CFTR causing congenital bilateral absence of the vas deferens in a Chinese pedigree. Li L; Qu X; Cui C; Feng K; Xia Y; Wan F; Ge H; Fang Y; Zhang C; Guo H Mol Genet Genomic Med; 2024 Jan; 12(1):e2364. PubMed ID: 38284450 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. [Mutations and polymorphisms in CFTR genes in infertile men with oligospermia or azoospermia]. Kusić J; Radojković D; Maletić V; Branković S; Savić A Srp Arh Celok Lek; 2002; 130(1-2):1-6. PubMed ID: 12073281 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Mutation spectrum of the CFTR gene in Taiwanese patients with congenital bilateral absence of the vas deferens. Wu CC; Alper OM; Lu JF; Wang SP; Guo L; Chiang HS; Wong LJ Hum Reprod; 2005 Sep; 20(9):2470-5. PubMed ID: 15905293 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. 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; 39(3):719-728. PubMed ID: 35119551 [TBL] [Abstract][Full Text] [Related]
19. Characterization of cystic fibrosis conductance transmembrane regulator gene mutations and IVS8 poly(T) variants in Portuguese patients with congenital absence of the vas deferens. Grangeia A; Niel F; Carvalho F; Fernandes S; Ardalan A; Girodon E; Silva J; Ferrás L; Sousa M; Barros A Hum Reprod; 2004 Nov; 19(11):2502-8. PubMed ID: 15333598 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]