Search Results - Hossein Najm-Abadi
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1
Review: Hearing Loss Genetics by Hossein Najm-Abadi, Kimia Kahrizi
Published 2005Call Number: Loading…Connect to this object online.
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2
Association of the Dopamine Transporter Gene (DAT1) Core Promotor Polymorphism-67T Allele with Schizophrenia by Mina Owhadi, Farbod Fadaei, Nazli Khodayari, Alireza Rahimi, Hossein Najm-Abadi
Published 2003Call Number: Loading…Connect to this object online.
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3
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 2006Call Number: Loading…Connect to this object online.
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4
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 2013Call Number: Loading…Connect to this object online.
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5
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
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6
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 2003Call Number: Loading…Connect to this object online.
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7
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 2010Call Number: Loading…Connect to this object online.
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8
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 2004Call Number: Loading…Connect to this object online.
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9
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 2006Call Number: Loading…Connect to this object online.
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10
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 2013Call Number: Loading…Connect to this object online.
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11
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 2005Call Number: Loading…Connect to this object online.
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