Nephro-Urology Monthly

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Linkage Analysis of Autosomal Dominant Polycystic Kidney Disease in Iranian Families through PKD1 and PKD2 DNA Microsatellite Markers

Fatemeh Hajizadeh Tafti 1 , Mohammad Reza Dehghani 2 , Ehsan Farashahi Yazd 3 , * , Maryam Golzadeh 4 , Mohammad Yahya Vahidi Mehrjardi 2 and Seyed Mehdi Kalantar 4 , 5
Authors Information
1 Medical Biotechnology Research Center, Ashkezar Branch, Islamic Azad University, Ashkezar, Yazd, IR Iran
2 Yazd Medical Genetics Research Center, Shahid Sadoughi University of Medical Sciences, Yazd, IR Iran
3 Stem Cell Biology Research Center, Yazd Reproductive Sciences Institute, Shahid Sadoughi University of Medical Sciences, Yazd, IR Iran
4 Recurrent Abortion Research Center, Yazd Reproductive Sciences Institute, Shahid Sadoughi University of Medical Sciences, Yazd, IR Iran
5 Department of Genetics, Faculty of Medicine, Shahid Sadoughi University of Medical Sciences, Yazd, IR Iran
Article information
  • Nephro-Urology Monthly: July 2017, 9 (4); e59996
  • Published Online: July 19, 2017
  • Article Type: Research Article
  • Received: November 29, 2016
  • Revised: March 19, 2017
  • Accepted: May 21, 2017
  • DOI: 10.5812/numonthly.59996

To Cite: Hajizadeh Tafti F, Dehghani M R, Farashahi Yazd E, Golzadeh M, Vahidi Mehrjardi M Y, et al. Linkage Analysis of Autosomal Dominant Polycystic Kidney Disease in Iranian Families through PKD1 and PKD2 DNA Microsatellite Markers, Nephro-Urol Mon. 2017 ; 9(4):e59996. doi: 10.5812/numonthly.59996.

Abstract
Copyright © 2017, Nephro-Urology Monthly. This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License (http://creativecommons.org/licenses/by-nc/4.0/) which permits copy and redistribute the material just in noncommercial usages, provided the original work is properly cited.
1. Background
2. Methods
3. Results
4. Discussion
Acknowledgements
Footnote
References
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