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زودتر از حد مجاز فراخوانی شد. این معمولاً نشاندهندهٔ اجرای کدی در افزونه یا پوسته است که خیلی زود اجرا شده است. ترجمهها باید در عملیات init
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زودتر از حد مجاز فراخوانی شد. این معمولاً نشاندهندهٔ اجرای کدی در افزونه یا پوسته است که خیلی زود اجرا شده است. ترجمهها باید در عملیات init
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\nAddress: Ardabil, Daneshghah st, Ardabil Complex University
\nAddress: Sarcheshmeh Sq., Masoumin Alley, Dr Maleki Dep, 1th floor
\nEDUCATION Start\/End Date
\nM.D. Tabriz University of Medical Sciences (TUOMS) Tabriz Start: 23\/09\/1988 End: 22\/10\/1995
\nPhD of Medical Genetics, Genetic Research Center (GRC), University of Social Welfare and
\nRehabilitation Sciences Start: 9\/02\/2010 End: 15\/01\/2015
\nPOST GRADUATE TRAINING Start\/End
\nPROFESSIONAL APPOINTMENTS Start\/End
\nAssistant Professor in Ardabil University of Medical Sciences
\nPRIVATE PRACTICE Start Date – End Date
\nMy Gene Lab, Medical Genetics Diagnostic Laboratory in Ardabil Start: 9\/02\/2017
\nMEDICAL AND SCIENTIFIC SOCIETIES Start Date – End Date
\nIranian Neurogenetics Society Start: 1\/07\/2017 End: 30\/12\/2021
\nAPPOINTMENTS Start\/End Date
\nArdabil University of Medical Sciences (ARUMS), Ardabil Deputy Minister in the medical disciplinary
\ncommittee
\nPOST DOCTORIAL CONFERENCES:
\nDate NAME OF CONFERENCE, City, Province or Stat
\nPUBLICATIONS:
\nGenetics of intellectual disability in consanguineous families
\nH Hu, K Kahrizi, L Musante, Z Fattahi, R Herwig, M Hosseini, C Oppitz, …
\nMolecular psychiatry 24 (7), 1027-1039
\n120 2019
\nIranome: a catalog of genomic variations in the Iranian population
\nZ Fattahi, M Beheshtian, M Mohseni, H Poustchi, E Sellars, SH Nezhadi, …
\nHuman mutation 40 (11), 1968-1984
\n59 2019
\nSpectrum of GJB2 (Cx26) gene mutations in Iranian Azeri patients with nonsyndromic
\nautosomal recessive hearing loss
\nB Davarnia, M Babanejad, Z Fattahi, N Nikzat, N Bazazzadegan, …
\nInternational journal of pediatric otorhinolaryngology 76 (2), 268-271
\n26 2012
\nIranome: A human genome variation database of eight major ethnic groups that live in Iran
\nand neighboring countries in the Middle East
\nMR Akbari, Z Fattahi, M Beheshtian, M Mohseni, H Poustchi, E Sellars, …
\nASHG Annual Meeting
\n9 2017
\nIdentification of a founder mutation for Pendred syndrome in families from northwest Iran
\nM Mohseni, A Honarpour, R Mozafari, B Davarnia, H Najmabadi, …
\nInternational journal of pediatric otorhinolaryngology 78 (11), 1828-1832
\n5 2014
\nThe Association between BRCA1 Expression and Breast Cancer Tumorogenesis
\nB Davarnia, P Mehdipour, M Arei, ASLSS HOSSEINI
\nJOURNAL OF ARDABIL UNIVERSITY OF MEDICAL SCIENCES (JAUMS) 12 (244), 132-139
\n5 2012
\nGJB2 mutations in Iranian Azeri population with autosomal recessive nonsyndromic hearing
\nloss (ARNSHL): First report of c. 238 C> A mutation in Iran
\nE Abbaspour Rodbaneh, M Panahi, B Rahimi, H Mokabber, R Farajollahi, …
\nJournal of Clinical Laboratory Analysis, e24024
\n2021
\nExome sequencing utility in defining the genetic landscape of hearing loss and novel\u2010gene
\ndiscovery in Iran
\nM Mohseni, M Babanejad, KT Booth, P Jamali, K Jalalvand, B Davarnia, …
\nClinical Genetics 100 (1), 59-78
\n2021
\nThe role of a novel TRMT1 gene mutation and rare GRM1 gene defect in intellectual disability
\nin two azeri families
\nH Davarniya, B.a, Hu, H.b, Kahrizi, K.a, Musante, L.b, Fattahi, Z.a …
\nPLoS ONE 10 (8), Article number e0129631
\n.
\nRESEARCH PROJECTS:
\n1. Identification of the genetic defects gland in situ congenital hypothyroidism
\n(GIS-CH) in Ardabil
\n2. Genetic mutation effects on Ochronosis Alkaptonuria families
\nPERSONAL DATA:
\nBehzad Davarnia, Head of the Medical Genetics and Pathology Department, Ardabil University of Medical
\nSciences, Ardabil, Iran,
\nMail: bdavarnia@gmail.com Phone: Tel.:+98(45)33272959 \u2018Fax: +98(45)33236277
\nDATE OF BIRTH: 25\/02\/1970
\nPLACE OF BIRTH: Ardabil, Iran
\nLANGUAGES: Azeri, Persian, English<\/p>\n<\/div><\/div><\/div>