Novel in-frame deletion in MFSD8 gene revealed by trio whole exome sequencing in an Iranian affected with neuronal ceroid lipofuscinosis type 7: a case report by Ali Hosseini Bereshneh, Masoud Garshasbi

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Novel compound heterozygous variants in XYLT1 gene caused Desbuquois dysplasia type 2 in an aborted fetus: a case report by Fatemeh Rajabi, Ali Hosseini Bereshneh, Mahboubeh Ramezanzadeh, Masoud Garshasbi

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Pharmacogenetics and Personalized Medicine in Pancreatic Cancer by Ali Hosseini Bereshneh, Fatemeh Morshedi, Mahsa Hematyar, Arastoo Kaki, Masoud Garshasbi

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Horizons of personalized medicine in breast cancer treatment: review article by Ali Hosseini Bereshneh, Danesh Soltani, Negar Veisi, Mohammad Khademi, Mohammad Hossein Modarressi

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Frequent Novel Variations Within MSH2 and MLH1 Genes in a Subset of Iranian Families With Hereditary Non-Polyposis Colorectal Cancer by Shadi Javan, Alireza Andalib, Ali Hosseini Bereshneh, Mohammad Hassan Emami, Rasul Salehi, Fatemeh Karami

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Methylation Assessment of Two DKK2 and DKK4 Genes in Oral Squamous Cell Carcinoma Patients by Sedigheh KHEIRANDISH, Nosratollah ESHGHYAR, Farzad YAZDANI, Pouyan AMINI SHAKIB, Ali HOSSEINI-BERESHNEH, Zahra NOURI, Ali KHEIRANDISH, Fatemeh KARAMI

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Characteristics of disease progression and genetic correlation in ambulatory Iranian boys with Duchenne muscular dystrophy by Gholamreza Zamani, Sareh Hosseinpour, Mahmoud Reza Ashrafi, Mahmoud Mohammadi, Reza Shervin Badv, Ali Reza Tavasoli, Masood Ghahvechi Akbari, Ali Hosseini Bereshneh, Reza Azizi Malamiri, Morteza Heidari

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