Items where Author is "Hashemzadeh Chaleshtori, Morteza."

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Article

Aali, Farzaneh. and Parchami Barjui, Shahrbanoo. and Aali, Faranak. and Raiesi, Somayeh. and Hashemzadeh Chaleshtori, Morteza. and Salehi, Ali. (2018) Investigation of the association between (CCTTT)n polymorphism in NOS2 gene and serum IgE level in patients with vernal keratoconjunctivitis in Chaharmahal va Bakhtiari Province. Gene Reports, 12.

Tabatabaiefar, Mohammad Amin. and Pourreza, Mohammad Reza. and Tahmasebi, Parisa. and Saki, Nader. and Hashemzadeh Chaleshtori, Morteza. and Salehi, Rasoul. and Mohammadi-Asl, Javad. (2018) A Novel Pathologic Variant in OTOF in an Iranian Family Segregating Hereditary Hearing Loss. Otolaryngology - Head and Neck Surgery (United States), 158 (6).

Asgharzadeh, Samira. and Tabatabaiefar, Mohammad Amin. and Mohammadi-Asl, Javad. and Hashemzadeh Chaleshtori, Morteza. (2018) A novel missense mutation in GIPC3 causes sensorineural hearing loss in an Iranian family revealed by targeted next-generation sequencing. International Journal of Pediatric Otorhinolaryngology, 108.

Reiisi, Somayeh. and Tabatabaiefar, Mohammad Amin. and Asgharzadeh, Samira. and Ghahremani, Mohammad Hossein. and Modarressi, Mohammad Hossein. and Tahmasebi, Parisa. and Abdollahnejad, Fatemeh. and Hashemzadeh Chaleshtori, Morteza. (2017) A novel TECTA mutation causes ARNSHL. International Journal of Pediatric Otorhinolaryngology, 92. pp. 88-93.

Zeinalian, Mehrdad. and Hashemzadeh Chaleshtori, Morteza. and Salehi, Rasoul. and Kazemi, Mohammad. and Emami, Mohammad Hassan. (2015) Tumor microsatellite instability and clinicopathologic features in Iranian colorectal cancer patients at risk for Lynch syndrome. JOURNAL OF RESEARCH IN MEDICAL SCIENCES, 20 (2). pp. 154-160.

Schrauwen, Isabelle. and Helfmann, Sarah. and Inagaki, Akira. and Predoehl, Friederike. and Tabatabaiefar, Mohammad Amin. and Magdalena Picher, Maria. and Sommen, Manou. and Seco, Celia Zazo and Oostrik, Jaap. and Kremer, Hannie. and Dheedene, Annelies. and Claes, Charlotte. and Fransen, Erik. and Hashemzadeh Chaleshtori, Morteza. and Coucke, Paul. and Lee, Amy. and Moser, Tobias. and Van Camp, Guy. (2012) A Mutation in CABP2, Expressed in Cochlear Hair Cells, Causes Autosomal-Recessive Hearing Impairment. AMERICAN JOURNAL OF HUMAN GENETICS, 91 (4). pp. 636-645.

Hashemzadeh Chaleshtori, Morteza. and Farrokhi, Effat. and Shayesteh, Farzad. and Modarresi, M and Shirani, M. and Roghani Dehkordi, F. and Ghatreh Samani, Keihan. and Mobini, Gholam Reza. and Banitalebi, Mehdi. and Ashrafi, Koorosh. and Shahrani, Mehrdad. and Parvin, Neda. (2011) Molecular characterization of familial hypercholesterolemia in Iranian patients. JOURNAL OF MEDICAL GENETICS, 45. S76.

Jenkins, Gareth J.S. and Hashemzadeh Chaleshtori, Morteza. and Song, Honglin. and Parry, James M. (1998) Mutation analysis using the restriction site mutation (RSM) assay. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis, 405 (2).

This list was generated on Thu Sep 19 01:09:19 2019 IRDT.