A Novel Mutation Associated with Dentinogenesis Imperfecta in a Patient with Hearing Loss: A Case Report by Farnoosh Naseri, Saeid Morovvati

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A novel mutation in the glutaryl‐CoA dehydrogenase gene (GCDH) in an Iranian patient affected with Glutaric acidemia type 1 by Sima Rayat, Saeid Morovvati

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Detecting Rare Triple Heteroplasmic Substitutions in the Mitochondrial DNA Control Region:A Potential Concern for Forensic DNA Studies by Saeid Morovvati, Ziba Morovvati, Reza Ranjbar

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A Study of Ribotype Patterns of Salmonella Enterica Serovar Enteritidis Strains Isolated in Tehran, Iran by Reza Ranjbar, Meysam Sarshar, Saeid Morovvati

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Cystinosis and two rare mutations in CTNS gene: two case reports by Sepideh Gholami Yarahmadi, Fatemeh Sarlaki, Saeid Morovvati

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Novel mutation in TENM3 gene in an Iranian patient with colobomatous microphthalmia by Sepideh Gholami Yarahmadi, Fatemeh Sarlaki, Saeid Morovvati

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Genotyping of 2 Cholesteryl Ester Transfer Protein Gene Variants Among Coronary Artery Disease Patients by Saeid Morovvati, Nima Kazemi Koohbanani, Iman Salahshouri Far, Fatemeh Karami

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Analysis of TMIE gene mutations including the first large deletion of exon 1 with autosomal recessive non-syndromic deafness by Sima Rayat, Mohammad Farhadi, Hessamaldin Emamdjomeh, Saeid Morovvati, Masoumeh Falah

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Waardenburg syndrome type 2A in a large Iranian family with a novel MITF gene mutation by Safoura Zardadi, Sima Rayat, Maryam Hassani Doabsari, Mohammad Keramatipour, Saeid Morovvati

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Mutation Analysis of ECM1 Gene in Two Related Iranian Patients Affected by Lipoid Proteinosis by Saeid Morovvati, Paniz Farshadyeganeh, Mojdeh Hamidizadeh, Ziba Morovvati, Samaneh Doost Mohammadi

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Hereditary Ataxia with a Novel Mutation in the Senataxin Gene: A Case Report by Ehsan Moghanloo, Ziba Morovvati, Maghsoud Seifi, Fatemeh Minoochehr, Saeid Morovvati, Shahram Teimourian

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A novel frameshift mutation in the EDA gene in an Iranian patient affected by X-linked hypohidrotic ectodermal dysplasia by Marzieh Rahbaran, Maryam Hassani Doabsari, Simindokht Salavitabar, Neda Mokhberian, Ziba Morovvati, Saeid Morovvati

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Mutation Detection in Activin A Receptor, Type I (ACVR1) Gene in Fibrodysplasia Ossificans Progressiva in An Iranian Family by Ziba Morovvati, Saeid Morovvati, Gholamhossein Alishiri, Seyed Hossein Moosavi, Reza Ranjbar, Yaser Bolouki Moghaddam

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Association study between polymorphisms in MIA3, SELE, SMAD3 and CETP genes and coronary artery disease in an Iranian population by Sima Rayat, Nasim Ramezanidoraki, Nima Kazemi, Mohammad H. Modarressi, Masoumeh Falah, Safoura Zardadi, Saeid Morovvati

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Four mutations in MITF, SOX10 and PAX3 genes were identified as genetic causes of waardenburg syndrome in four unrelated Iranian patients: case report by Safoura Zardadi, Sima Rayat, Maryam Hassani Doabsari, Aliagha Alishiri, Mohammad Keramatipour, Zeynab Javanfekr Shahri, Saeid Morovvati

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Novel homozygous variants in the TMC1 and CDH23 genes cause autosomal recessive nonsyndromic hearing loss by Safoura Zardadi, Ehsan Razmara, Golareh Asgaritarghi, Ehsan Jafarinia, Fatemeh Bitarafan, Sima Rayat, Navid Almadani, Saeid Morovvati, Masoud Garshasbi

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