Items where Author is "Alipour, Paria."

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Article

Tabatabaiefar, Mohammad Amin. and Alipour, Paria. and Pourahmadiyan, Azam. and Fattahi, Najmeh. and Shariati, Laleh. and Golchin, Neda. and Mohammadi-Asl, Javad. (2017) A novel pathogenic variant in an Iranian Ataxia telangiectasia family revealed by next-generation sequencing followed by in silico analysis. JOURNAL OF THE NEUROLOGICAL SCIENCES, 379. pp. 212-216.

Pourahmadiyan, Azam. and Tabatabaiefar, Mohammad Amin. and Reiisi, Somayeh. and Alipour, Paria. and Fattahi, Najmeh. and Hashemzadeh-Chaleshtori, Morteza. (2016) Genetic linkage analysis of DFNB40 and DFNB48 loci in families with autosomal recessive non-syndromic hearing loss (ARNSHL) from western provinces of Iran. Journal of Isfahan Medical School, 34 (374).

Pourahmadiyan, Azam. and Tabatabaiefar, Mohammad Amin. and Reiisi, Somayeh. and Alipour, Paria. and Fattahi, Najmeh. and Hashemzadeh-Chaleshtori, Morteza. (2016) Genetic linkage analysis of DFNB7/11 locus in patients with autosomal recessive non syndromic hearing loss from Hamedan province. journal of shahrekord university of medical sciences, 18 (3).

Fattahi, Najmeh. and Tabatabaiefar, Mohammad Amin. and Reeisi, Somayeh. and Alipour, Paria. and Pourahmadian, Azam. and Hashemzadeh-Chaleshtori, Morteza. (2015) Genetic linkage analysis of DFNB59 loci involved in autosomal recessive non-syndromic hearing loss (ARNSHL) in western provinces of Iran. journal of shahrekord university of medical sciences, 17 (4).

Alipour, Paria. and Tabatabaiefar, Mohammad Amin. and Reiisi, Somayeh. and Fattahi, Najmeh. and Pourahmadian, Azam. and Hashemzadeh-Chaleshtori, Morteza. (2015) Genetic linkage analysis of the DFNB63 locus in families with autosomal recessive nonsyndromic hearing loss from Hamadan and Kohgiluyeh and Boyer-Ahmad Provinces, Iran. Journal of Isfahan Medical School, 33 (346). pp. 1308-1317.

This list was generated on Wed Apr 25 01:06:06 2018 IRDT.