A Novel Mutation in ERCC8 Gene Causing Cockayne Syndrome by Maryam Taghdiri, Maryam Taghdiri, Hassan Dastsooz, Majid Fardaei, Majid Fardaei, Majid Fardaei, Sanaz Mohammadi, Mohammad Ali Farazi Fard, Mohammad Ali Faghihi

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Commentary: Profiling of UGT1A1*6, UGT1A1*60, UGT1A1*93, and UGT1A1*28 Polymorphisms in Indonesian Neonates With Hyperbilirubinemia Using Multiplex PCR Sequencing by Mohammad Reza Heydari, Majid Fardaei

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DNA Sequence Fragment Containing C to A Mutation as a Convenient Mutation Standard for DHPLC Analysis by Hassan Dastsooz, Nazanin Vahedi, Majid Fardaei

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Expression Analysis of Multiple Genes May Involve in Antimony Resistance among Leishmania major Clinical Isolates from Fars Province, Central Iran by Nafiseh GHOBAKHLOO, Mohammad Hossein MOTAZEDIAN, Majid FARDAEI

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A Novel Missense Mutation in CLCN1 Gene in a Family with Autosomal Recessive Congenital Myotonia by Mohammad Miryounesi, Soudeh Ghafouri-Fard, Majid Fardaei

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MSX1 Mutation in Witkop Syndrome; A Case Report by Faezeh Ghaderi, Somaye Hekmat, Reza Ghaderi, Majid Fardaei

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Sequencing of third exon of IGF1 gene in sheep by Saeideh Sajjadi, Mohammad Reza Bahreini Behzadi, Majid Fardaei

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The association between FTO rs9939609 gene polymorphism and anthropometric indices in adults by Mahsa Mehrdad, Majid Fardaei, Mohammad Fararouei, Mohammad Hassan Eftekhari

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The Effect of Short-Term Mediterranean-DASH Intervention for Neurodegenerative Delay (MIND) Diet on Hunger Hormones, Anthropometric Parameters, and Brain Structures in Middle-Aged... by Golnaz Arjmand, Mojtaba Abbas-Zadeh, Majid Fardaei, Mohammad Hassan Eftekhari

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VSX1 and SOD1 mutation screening in patients with keratoconus in the South of Iran by Mahmood Nejabat, Payam Naghash, Hassan Dastsooz, Sanaz Mohammadi, Mohsen Alipour, Majid Fardaei

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Author's reply by Mahmood Nejabat, Payam Naghash, Hassan Dastsooz, Sanaz Mohammadi, Mohsen Alipour, Majid Fardaei

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Founder Effect of KHDC3L, p.M1V Mutation, on Iranian Patients with Recurrent Hydatidiform Moles by Jafar Fallahi, Zahra Anvar, Vahid Razban, Mozhdeh Momtahan, Bahia Namavar-Jahromi, Majid Fardaei

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Novel mutations in PANK2 and PLA2G6 genes in patients with neurodegenerative disorders: two case reports by Hassan Dastsooz, Hamid Nemati, Mohammad Ali Farazi Fard, Majid Fardaei, Mohammad Ali Faghihi

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Association of FTO rs9939609 polymorphism with serum leptin, insulin, adiponectin, and lipid profile in overweight adults by Mahsa Mehrdad, Saeid Doaei, Maryam Gholamalizadeh, Majid Fardaei, Mohammad Fararouei, Mohammad Hassan Eftekhari

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Segmental Duplications as a Complement Strategy to Short Tandem Repeats in the Prenatal Diagnosis of Down Syndrome by Mohammad Reza Miri, Jamileh Saberzadeh, Abbas Behzad Behbahani, Mohammad Bagher Tabei, Mohsen Alipour, Majid Fardaei

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Further delineation of the phenotype caused by a novel large homozygous deletion of GRID2 gene in an adult patient by Maryam Taghdiri, Atie Kashef, Golemaryam Abbassi, Azadeh Moshtagh, Neda Sadatian, Majid Fardaei, Kimia Najafi, Roxana Kariminejad

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An immunocompetent patient with a nonsense mutation in NHEJ1 gene by Hossein Esmaeilzadeh, Mohammad Reza Bordbar, Zahra Hojaji, Parham Habibzadeh, Dorna Afshinfar, Mohammad Miryounesi, Majid Fardaei, Mohammad Ali Faghihi

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Inferior Spear-like Lens Opacity as a Sign of Keratoconus by Ramin Salouti, Amir Khosravi, Majid Fardaei, Mohammad Zamani, MD Mahmoud Nejabat, Maryam Ghoreyshi, Mahboobeh Yazdanpanah, Kia Salouti, M. Hossein Nowroozzadeh

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The First Case of a Small Supernumerary Marker Chromosome 18 in a Klinefelter Fetus: A Case Report by Jamileh Saberzadeh, Mohammad Reza Miri, Mehdi Dianatpour, Abbas Behzad Behbahani, Mohammad Bagher Tabei, Mohsen Alipour, Mohammad Ali Faghihi, Majid Fardaei

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