Zoekresultaten - Kimia Kahrizi

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

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

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

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

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

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

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

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

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

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

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

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Genetic Causes of Mental Retardation in Bushehr Province door 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

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Classification of Neuromuscular Disorders Based an Clinical Criteria , Molocular and Immunohistochemisty Analysis in Tehran Pateints door 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

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Genetic Causes of Mental Retardation in Golestan Province door 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

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