CAD gene and early infantile epileptic encephalopathy-50; three Iranian deceased patients and a novel mutation: case report von Yarahmadi, Sepideh Gholami, Morovvati, Saeid

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Evaluation of mtDNA common deletion in esophageal squamous cell carcinoma von Ghadyani, Fatemeh, Sharif, Shahrbanoo, Morovvati, Saeid

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

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

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

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

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

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

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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 von Zardadi, Safoura, Rayat, Sima, Doabsari, Maryam Hassani, Alishiri, Aliagha, Keramatipour, Mohammad, Shahri, Zeynab Javanfekr, Morovvati, Saeid

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

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

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

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

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Mutation detection and inhibitor risk in Iranian patients with Hemophilia A: Six novel mutations von Nasirnejad Sola, Farzaneh, Morovvati, Saeid, Sabetghadam Moghadam, Mitra, Entezari, Malihe

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

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

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

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Detecting rare triple heteroplasmic substitutions in the mitochondrial DNA control region: a potential concern for forensic DNA studies von Morovvati, Saeid, Morovvati, Ziba, Ranjbar, Reza

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Model-based cost estimation for infrastructure projects: a case study von Morovvati, Saeid

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Genetic study of a family with affected members with Waardenburg syndrome type 4 without Hirschsprung disease von Moghadam, Mitra Sabetghadam, Rayat, Sima, Morovvati, Saeid

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