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 2013-10-01

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 2013-01-01

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 2005-10-01

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 2010-10-01

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 2006-10-01

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 2012-04-01

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 2005-01-01

Review: Hearing Loss Genetics

by Hossein Najm-Abadi, Kimia Kahrizi
Published 2005-04-01

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 2010-01-01

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 2003-12-01

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 2006-04-01

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

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 2004-06-01