Identification of a Novel Frameshift Mutation in the TECTA Gene in an Iranian Family With Autosomal Nonsyndromic Hearing Loss von Mohammadi-Asl, Javad, Saki, Nader, Karimi, Majid, Ghanbari Mardasi, Farideh

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Digenic Mutations in Junctional Epidermolysis Bullosa in An Iranian Family von Riahi, Kourosh, Farideh Ghanbari Mardasi, Talebi, Farah, Jasemi, Farzad, Javad Mohammadi Asl

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Identification of a Novel WFS1 Mutation Using the Whole Exome Sequencing in an Iranian Pedigree with Autosomal Dominant Hearing Loss von Mohammadi-Asl, Javad, Saki, Nader, Dehdashtiyan, Masoud, Neissi, Mostafa, Ghanbari Mardasi, Farideh

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Identification of Novel PTPRQ and MYO1A Mutations in An Iranian Pedigree with Autosomal Recessive Hearing Loss von Talebi, Farah, Ghanbari Mardasi, Farideh, Mohammadi Asl, Javad, Tizno, Saeed, Najafvand Zadeh, Marziye

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Identification of A Novel Missense Mutation in The Norrie Disease Gene: The First Molecular Genetic Analysis and Prenatal Diagnosis of Norrie Disease in An Iranian Family von Talebi, Farah, Ghanbari Mardasi, Farideh, Mohammadi Asl, Javad, Lashgari, Ali, Farhadi, Freidoon

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Next-Generation Sequencing Reveals One Novel Missense Mutation in COL1A2 Gene in an Iranian Family with Osteogenesis imperfecta von Talebi, Farah, Ghanbari Mardasi, Farideh, Javad, Mohammadi Asl, Amir Hooshang, Bavarsad, Masoumeh, Salehi Kambo

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Identification of a novel missence mutation in FGFR3 gene in an Iranian family with LADD syndrome by Next-Generation Sequencing von Talebi, Farah, Ghanbari Mardasi, Farideh, Mohammadi Asl, Javad, Bavarsad, Amir Hooshang, Tizno, Saeed

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Association of HLA-DR2-Related Haplotype (HLA-DRB501-DRB11501-DQB10602) in Patients with Multiple Sclerosis in Khuzestan Province von Delfan, Nooshin, Galehdari, Hamid, Ghanbari Mardasi, Farideh, Zabihi, Rezvan, Latifi Pakdehi, Tahereh, Seifi, Tahereh, Majdinasab, Nastaran

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Identification of a Novel Non-Stop Mutation in PDE6C Gene in an Iranian Family With Con-Rod Dystrophy von Nasiri, Shahram, Talebi, Farah, Javad Mohammadi Asl, Farideh Ghanbari Mardasi

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Identification of A Novel Missense Mutation in The Norrie Disease Gene: The First Molecular Genetic Analysis and Prenatal Diagnosis of Norrie Disease in An Iranian Family von Talebi, Farah, Farideh Ghanbari Mardasi, Javad Mohammadi Asl, Lashgari, Ali, Farhadi, Freidoon

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Next-generation sequencing identifies three novel missense variants in ILDR1 and MYO6 genes in an Iranian family with hearing loss with review of the literature von Talebi, Farah, Mardasi, Farideh Ghanbari, Asl, Javad Mohammadi, Sayahi, Masoomeh

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Mutational spectrum of the CYP1B1 gene in Iranain primary congenital glaucoma family von Talebi, Farah, Mardasi, Farideh Ghanbari, Asl, Javad Mohammadi, Lashgari, Ali

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Association of HLA-DR2-Related Haplotype (HLA-DRB501-DRB11501-DQB10602) in Patients with Multiple Sclerosis in Khuzestan Provinc von Delfan, Nooshin, Galehdari, Hamid, Mardasi, Farideh Ghanbari, Zabihi, Rezvan, Pakdehi, Tahereh Latifi, Seifi, Tahereh, Majdinasab, Nastaran

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Association of Resistin Gene Polymorphism with Type 2 Diabetes in Khuzestan Province von Mohammadi Asl, Javad, Zakerkish, Mehrnoosh, Ghanbari Mardasi, Farideh, Ghaffari, Mohammad Ali, Rezazadeh, Mahin

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Thalassemia Spectrum and Prenatal Diagnosis among Voluntary Couples in Shushtar City, during a Five Year Period von Sayahi, Masoomeh, Ghanbari Mardasi, Farideh, Salehi Kambo, Masoomeh

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Association of human leukocyte antigen-DRB haplotype in multiple sclerosis population of Khuzestan, Iran von Delfan, Nooshin, Galehdari, Hamid, Shafiei, Mohammad, Ghanbari-Mardasi, Farideh, Latifi, Tahereh, Majdinasab, Nastaran, Seifi, Tahereh

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The Relationship Between Promoter Methylation of RASSF1A Gene and Prognosis of Patients Affected with Breast Cancer in Khuzestan Province von Mohammadi Asl, Javad, Ghanbari Mardasi, Farideh, Saki, Ghasem, Rahim, Fakher, Rashidi, Iran, Ranjbari, Nastaran, Kheradmand, Parvin, Abromand, Mohammad, ghavabesh, Jasem, Fazeli, Kolsoum

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Association of human leukocyte antigen-DRB haplotype in multiple sclerosis population of Khuzestan, Iran von Delfan, Nooshin, Galehdari, Hamid, Shafiei, Mohammad, Ghanbari-Mardasi, Farideh, Latifi, Tahereh, Majdinasab, Nastaran, Seifi, Tahereh

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PDigenic Mutations in Junctional Epidermolysis Bullosa in An Iranian Family von Riahi, Kourosh, Ghanbari Mardasi, Farideh, Talebi, Farah, Jasemi, Farzad, Mohammadi Asl, Javad

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Identification of a Novel WFS1 Mutation Using the Whole Exome Sequencing in an Iranian Pedigree with Autosomal Dominant Hearing Loss von Mohammadi-Asl, Javad, Saki, Nader, Dehdashtiyan, Masoud, Neissi, Mostafa, Ghanbari Mardasi, Farideh

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