Indan Journal of Medical Research Indan Journal of Medical Research Indan Journal of Medical Research Indan Journal of Medical Research
  Home About us Editorial board Search Ahead of print Current issue Archives Submit article Instructions Subscribe Contacts Login  
  Home Print this page Email this page Small font sizeDefault font sizeIncrease font size Users Online: 238       

    Article Cited by others

ORIGINAL ARTICLE

Cystic fibrosis transmembrane conductance regulator (CFTR) gene abnormalities in Indian males with congenital bilateral absence of vas deferens & renal anomalies

Gajbhiye Rahul, Kadam Kaushiki, Khole Aalok, Gaikwad Avinash, Kadam Seema, Shah Rupin, Kumaraswamy Rangaswamy, Khole Vrinda

Year : 2016| Volume: 143| Issue : 5 | Page no: 616-623

   This article has been cited by
 
1 Expanding the phenotypic and genetic spectrum of Chinese patients with congenital absence of vas deferens bearing CFTR and ADGRG2 alleles
P. Yuan,Z. K. Liang,H. Liang,L. Y. Zheng,D. Li,J. Li,J. Zhang,J. Tian,L. H. Lai,K. Zhang,Z. Y. He,Q. X. Zhang,W. J. Wang
Andrology. 2019;
[Pubmed]  [Google Scholar] [DOI]
2 A novel mutation (-195C>A) in the promoter region of CFTR gene is associated with Chinese Congenital Bilateral Absence of Vas Deferens (CBAVD)
Jiarong Feng,Xiao Wu,Yanan Zhang,Xiaojian Yang,Gongchao Ma,Shitao Chen,Shaoge Luo,Yan Zhang
Gene. 2019; : 144007
[Pubmed]  [Google Scholar] [DOI]
3 The CFTR gene mild variants poly-T, TG repeats and M470V detection in Indian men with congenital bilateral absence of vas deferens
A. Gaikwad,S. Khan,S. Kadam,K. Kadam,V. Dighe,R. Shah,V. Kulkarni,R. Kumaraswamy,R. Gajbhiye
Andrologia. 2017; : e12858
[Pubmed]  [Google Scholar] [DOI]

 

Read this article