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Last Posted: Mar 15, 2023

• Correlation between CFTR variants and outcomes of ART in patients with CAVD in Central China.
  Qu Xiaowei, et al. Scientific reports 2023 0 (1) 64
• [Homozygous 5T alleles, clinical presentation and genetic analysis within a family with congenital bilateral absence of the vas deferens].
  Feng J R, et al. Zhonghua yi xue za zhi 2018 0 (18) 1414-1418
• SLC9A3 Affects Vas Deferens Development and Associates with Taiwanese Congenital Bilateral Absence of the Vas Deferens.
  Wu Yi-No, et al. BioMed research international 2019 0 3562719
• Characterization of clinical and genetic spectrum of Chinese patients with cystic fibrosis.
  Liu Keqiang, et al. Orphanet journal of rare diseases 2020 0 (1) 150
• Andrological findings in infertile men with two (biallelic) CFTR mutations: results of a multicentre study in Germany and Austria comprising 71 patients.
  Rudnik-Schöneborn S, et al. Human reproduction (Oxford, England) 2020 0 (3) 551-559
• Loss-of-function CFTR p.G970D missense mutation might cause congenital bilateral absence of the vas deferens and be associated with impaired spermatogenesis.
  Hou Jian-Wen, et al. Asian journal of andrology 2022 6
• Genetic analysis and intracytoplasmic sperm injection outcomes of Chinese patients with congenital bilateral absence of vas deferens.
  Cheng Hongbo, et al. Journal of assisted reproduction and genetics 2022 2
• Current updates and future perspectives in the evaluation of azoospermia: A systematic review.
  Punjani Nahid et al. Arab journal of urology 2021 19(3) 206-214
• [Correlation between CFTR 5T polymorphisms and the risk of congenital bilateral absence of the vas deferens].
  Zhao Guo-Guo, et al. Zhonghua nan ke xue = National journal of andrology 2019 3 (3) 231-237
• Genetic diagnosis and sperm retrieval outcomes for Chinese patients with congenital bilateral absence of vas deferens.
  Wang Hongxiang, et al. Andrology 2020 2
• Congenital bilateral absence of the vas deferens (CBAVD): do genetic disorders modify assisted reproductive technologies outcomes?
  Gallego Ángel, et al. Archivos espanoles de urologia 2019 12 (10) 1038-1042
• The association between variants in the CFTR gene and nonobstructive male infertility: A meta-analysis.
  Yang Luchen, et al. Andrologia 2019 12 e13475
• 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 Fatemeh, et al. Iranian biomedical journal 2018 7
• 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 Song, et al. Gene 2018 6
• Pathogenic role of ADGRG2 in CBAVD patients replicated in Chinese population.
  Yang B, et al. Andrology 2017 8
• The CFTR gene mild variants poly-T, TG repeats and M470V detection in Indian men with congenital bilateral absence of vas deferens.
  Gaikwad A, et al. Andrologia 2017 8
• Truncating Mutations in the Adhesion G Protein-Coupled Receptor G2 Gene ADGRG2 Cause an X-Linked Congenital Bilateral Absence of Vas Deferens.
  Patat Olivier, et al. American journal of human genetics 2016 8 (2) 437-42
• Molecular screening of CFTR gene in Egyptian patients with congenital bilateral absence of the vas deferens: a preliminary study.
  Fathy M, et al. Andrologia 2016 3
• Meta-analyses of 4 CFTR variants associated with the risk of the congenital bilateral absence of the vas deferens.
  Xu Xuting, et al. Journal of clinical bioinformatics 2014 0 11
• Clinical and prognostic importance of chromosomal abnormalities, Y chromosome microdeletions, and CFTR gene mutations in individuals with azoospermia or severe oligospermia.
  Ocak Zeynep, et al. Turkish journal of medical sciences 2014 0 (2) 347-51
• Preimplantation genetic diagnosis for cystic fibrosis: the Montpellier center's 10-year experience.
  
• Increased frequency of CFTR gene mutations identified in Indian infertile men with non-CBAVD obstructive azoospermia and spermatogenic failure.
  Sharma Himanshu, et al. Gene 2014 9 (1) 43-7
• The CFTR M470V, intron 8 poly-T, and 8 TG-repeats detection in Chinese males with congenital bilateral absence of the vas deferens.
  Du Qiang, et al. BioMed research international 2014 0 689185
• p.Arg75Gln, a CFTR variant involved in the risk of CFTR-related disorders?
  Martinez Brigitte, et al. Journal of human genetics 2014 4 (4) 206-10
• CFTR p.Arg117His associated with CBAVD and other CFTR-related disorders.
  Thauvin-Robinet C, et al. Journal of medical genetics 2013 2
• The CFTR polymorphisms poly-T, TG-repeats and M470V in Chinese males with congenital bilateral absence of the vas deferens.
  Ni Wu-Hua, et al. Asian journal of andrology 2012 9 (5) 687-90
• The D1152H cystic fibrosis mutation in prenatal carrier screening, patients and prenatal diagnosis.
  Peleg Leah, et al. Journal of medical screening 2011 0 (4) 169-72
• Molecular screening of the CFTR gene in Mexican patients with congenital absence of the vas deferens.
  Saldaña-Alvarez Yolanda, et al. Genetic testing and molecular biomarkers 2012 4 (4) 292-6
• CFTR mutations in men with congenital bilateral absence of the vas deferens (CBAVD): a systemic review and meta-analysis.
  Yu Jianmin, et al. Human reproduction (Oxford, England) 2012 1 (1) 25-35
• Screening of ?F508 mutation and IVS8-poly T polymorphism in CFTR gene in Tunisian infertile men without CBAVD.
  Ghorbel M, et al. Andrologia 2012 5 376-82

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