Showing 1 - 7 results of 7 for search 'S Arzhangi', query time: 0.03s Refine Results
  1. 1
    Investigating the Contribution of SocioPhysical Structure of Neighborhoods on Residents’ Sense of Attachment

    Investigating the Contribution of SocioPhysical Structure of Neighborhoods on Residents’ Sense of Attachment by Navid KHALEGHIMOGHADDAM, Sara ARZHANGI, Narges RAJAEIPOUR

    Published 2023-09-01
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    Article
  2. 2
    The Impact of Time-use Training on the Quality of Time Management in the Mothers of Children With Intellectual Disabilities

    The Impact of Time-use Training on the Quality of Time Management in the Mothers of Children With Intellectual Disabilities by Sanaz Arzhangi, Meimanat Hosseini, Samaneh Hosseinzadeh, Mansoureh Zagheri Tafreshi

    Published 2020-06-01
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  3. 3
    Prevalence Study of GJB2 Gene Mutations in Iranian Ethnics

    Prevalence Study of GJB2 Gene Mutations in Iranian Ethnics by Kimia Kahrizi, Niloufar Bazzaz-Zadegan, Marzieh Mohseni, Noushin Nik-Zaat, Khadijeh Jalalvand, Yaser Riaz-el Hosseini, Yousef Shafeghati, Sanaz Arzhangi, Khalil Javan, Hosein Najmabadi

    Published 2007-10-01
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  4. 4
    Relative Frequency of 35delG Mutation in GJB2 Gene in Autosomal Recessive Non-Syndromic Hearing Loss (ARNSHL) Patients in Kerman Population

    Relative Frequency of 35delG Mutation in GJB2 Gene in Autosomal Recessive Non-Syndromic Hearing Loss (ARNSHL) Patients in Kerman Population by N Bazazzadegan, N Mirhoseini, H Ziaaddini, AR Asadi, K Kahrizi, S Arzhangi, A Astani, M Mohseni, Y Riazalhosseini, M Nejat, Kh Jalalvand, RJH Smith, C Nishimura, H Najmabadi

    Published 2004-07-01
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  5. 5
    Whole genome sequencing identifies a duplicated region encompassing Xq13.2q13.3 in a large Iranian family with intellectual disability

    Whole genome sequencing identifies a duplicated region encompassing Xq13.2q13.3 in a large Iranian family with intellectual disability by Sepideh Mehvari, Farzaneh Larti, Hao Hu, Zohreh Fattahi, Maryam Beheshtian, Seyedeh Sedigheh Abedini, Sanaz Arzhangi, Hans‐Hilger Ropers, Vera M. Kalscheuer, Daniel Auld, Kimia Kahrizi, Yasser Riazalhosseini, Hossein Najmabadi

    Published 2020-10-01
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  6. 6
    P292: Contribution of rare variants in the development of familial premature coronary artery disease in a cohort of cardiac patients

    P292: Contribution of rare variants in the development of familial premature coronary artery disease in a cohort of cardiac patients by Sepideh Mehvari, Nahid Karimian Fathi, Maryam Asadnezhad, Sanaz Arzhangi, Saeed Sadeghian, Mohammadali Boroumand, Fatemeh Shokohizadeh, Elham Rostami, Rahnama Boroumand, Reza Malekzadeh, Yasser Riazalhosseini, Mohammadreza Akbari, Mark Lathrop, Hossein Najmabadi, Kaveh Hosseini, Kimia Kahrizi

    Published 2024-01-01
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  7. 7
    Distinct genetic variation and heterogeneity of the Iranian population.

    Distinct genetic variation and heterogeneity of the Iranian population. by Zohreh Mehrjoo, Zohreh Fattahi, Maryam Beheshtian, Marzieh Mohseni, Hossein Poustchi, Fariba Ardalani, Khadijeh Jalalvand, Sanaz Arzhangi, Zahra Mohammadi, Shahrouz Khoshbakht, Farid Najafi, Pooneh Nikuei, Mohammad Haddadi, Elham Zohrehvand, Morteza Oladnabi, Akbar Mohammadzadeh, Mandana Hadi Jafari, Tara Akhtarkhavari, Ehsan Shamsi Gooshki, Aliakbar Haghdoost, Reza Najafipour, Lisa-Marie Niestroj, Barbara Helwing, Yasmina Gossmann, Mohammad Reza Toliat, Reza Malekzadeh, Peter Nürnberg, Kimia Kahrizi, Hossein Najmabadi, Michael Nothnagel

    Published 2019-09-01
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