Showing 1 - 14 results of 14 for search 'Kimia Kahrizi', query time: 0.11s Refine Results
  1. 1
    Review: Hearing Loss Genetics

    Review: Hearing Loss Genetics by Hossein Najm-Abadi, Kimia Kahrizi

    Published 2005
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  2. 2
    Genetic Causes of Putative Autosomal Recessive Intellectual Disability Cases in Hamedan Province

    Genetic Causes of Putative Autosomal Recessive Intellectual Disability Cases in Hamedan Province by Milad Bastami, Elaheh Papari, Seyedeh Sedigheh Abedini, Kimia Kahrizi, Hossein Najmabadi

    Published 2012
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  3. 3
    Intellectual disability associated with craniofacial dysmorphism due to POLR3B mutation and defect in spliceosomal machinery

    Intellectual disability associated with craniofacial dysmorphism due to POLR3B mutation and defect in spliceosomal machinery by Mostafa Saghi, Kolsoum InanlooRahatloo, Afagh Alavi, Kimia Kahrizi, Hossein Najmabadi

    Published 2022
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  4. 4
    GJB2 Mutations Screening in Autosomal Recessive Non-Syndrome Deaf Patients of Khouzestan Province

    GJB2 Mutations Screening in Autosomal Recessive Non-Syndrome Deaf Patients of Khouzestan Province by Kimia Kahrizi, Ali Sajjadi, Marzieh Mohseni, Yaser Riaz-el Hosseini, Hossein Najm-Abadi

    Published 2006
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  5. 5
    Investigation Genetic Causes Of Hereditary Intellectual Disability in Ahvaz (2011-2012)

    Investigation Genetic Causes Of Hereditary Intellectual Disability in Ahvaz (2011-2012) by Saeedeh Akbari-Mobarakeh, Elinaz Akbari-Azar, Mohammad Reza Ebrahimpour, Hossein Najm-Abadi, Kimia Kahrizi

    Published 2013
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  6. 6
    Report of Iranian Family with Pendred Syndrome with New Mutation T420I, and Multiply Heterozygous New Mutation T420I and 1197delT

    Report of Iranian Family with Pendred Syndrome with New Mutation T420I, and Multiply Heterozygous New Mutation T420I and 1197delT by Hossein Najm-Abadi, Kimia Kahrizi, Marzieh Mohseni, Fatemeh Sadat Esteghamat, Sanaz Arzhangi, Richard Smith

    Published 2005
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  7. 7
    Case Report: First Report of Mutation in Col 11A2 Gene in an Iranian Family with Autosomal Rrecessive Non-Syndromic Hearing Loss

    Case Report: First Report of Mutation in Col 11A2 Gene in an Iranian Family with Autosomal Rrecessive Non-Syndromic Hearing Loss by Kimia Kahrizi, Ahmad Daneshi, Yasser Riaz-el Hosseini, Carla Nishimora, Richard Smith, Hossein Najm-Abadi

    Published 2003
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  8. 8
    Haplotype Analysis of Seven Non-Syndromeic Autosomal Recessive Hearing Loss Loci in Iranian Families

    Haplotype Analysis of Seven Non-Syndromeic Autosomal Recessive Hearing Loss Loci in Iranian Families by Ramak Badr, Bahareh Shoja-Saffar, Niloofar Bazzaz-Zadegan, Khadijeh Jalalvand, Kimia Kahrizi, Hossein Najm-Abadi

    Published 2010
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  9. 9
    Screening of Autosomal Recessive Non-Syndromic Hearing Loss gor GJB2 Mutations

    Screening of Autosomal Recessive Non-Syndromic Hearing Loss gor GJB2 Mutations by Atefeh Khosh-Aeen, Fatemeh Pourfatemi, Kimia Kahrizi, Yaser Riaz-Alhosseini, Marziyeh Mohseni, Niloufar Bazzaz-Zadegan, Nooshin Nik-Zaat, Hossein Najm-Abadi

    Published 2004
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  10. 10
    Linkage Analysis for 50 Iranian Families with Autosomal Recessive Non-Syndromic Hearing Loss for DFNB21 Locus

    Linkage Analysis for 50 Iranian Families with Autosomal Recessive Non-Syndromic Hearing Loss for DFNB21 Locus by Parisa Imani-Raad, Kimia Kahrizi, Niloufar Bazzaz-Zadegan, Marzieh Mohseni, Golnaz As'adi, Noushin Nik-Zaat, Fatemeh Sadat Esteghamat, Hossein Najm-Abadi

    Published 2006
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  11. 11
    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
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  12. 12
    Genetic Causes of Mental Retardation in Bushehr Province

    Genetic Causes of Mental Retardation in Bushehr Province by Elaheh Papari, Akram Farhadi, Ma'soumeh Hosseini, Seyyedeh Sedigheh A'bedini, Marzieh Mohseni, Sousan Bani-Hashemi, Sanaz Arjangi, Farkhndeh Behjati, Kimia Kahrizi, Hossein Najm-Abadi

    Published 2013
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  13. 13
    Classification of Neuromuscular Disorders Based an Clinical Criteria , Molocular and Immunohistochemisty Analysis in Tehran Pateints

    Classification of Neuromuscular Disorders Based an Clinical Criteria , Molocular and Immunohistochemisty Analysis in Tehran Pateints by Kimia Kahrizi, Yousef Shafaghati, Elaheh Keyhani, Mandana Hassan-Zad, Mojtaba A'zimiyan, Fereidoun Layeghi, Afshin Vojdani-Rowshan, John Andoni-Ortizbera, Daniel Hentay, Hossein Najm-Abadi

    Published 2005
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  14. 14
    Genetic Causes of Mental Retardation in Golestan Province

    Genetic Causes of Mental Retardation in Golestan Province by Hossein Darvish, Saghar Ghasemi-Firouzabadi, Gholam Reza Bahrami-Monajemi, Ideh Bahman, Marziyeh Mohseni, Mohammad Javad Soltani-Banavandi, Sousan Banihashemi , Sanaz Arjangi, Farkhondeh Behjati, Kimia Kahrizi, Hossein Najmabadi

    Published 2010
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