Items where Author is "Akbari, M.T."

Up a level
Export as [feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Item Type | No Grouping
Jump to: Article
Number of items: 9.


Jafari Ghahfarokhi, H. and Ashoori, S. and Akbari, M.T. and Lotfizadeh, M. and Karimi, A. and Teimori, H. (2014) ZAP70 Expression Within del6q21, del11q13 and del17p13 Cytogenetic Subgroups of Iranian Patients with Chronic Lymphocytic Leukemia. IRANIAN RED CRESCENT MEDICAL JOURNAL, 16 (11).

Teimori, H. and Ashoori, S. and Akbari, M.T. and Mojtabavi Naeini, M. and Hashemzade Chaleshtori, M. (2013) FISH Analysis for del6q21 and del17p13 in B-cell Chronic Lymphocytic Leukemia in Iranians. IRANIAN RED CRESCENT MEDICAL JOURNAL, 15 (2). pp. 107-112.

Zohour, M.M. and Akbari, M.T. and Chaleshtori, M.H. (2012) Frequency of the mitochondrial A1555G mutation in Iranian patients with non-syndromic hearing impairment. Indian Journal of Science and Technology, 5 (10). pp. 3378-3383.

Montazer Zohour, M. and Tabatabaiefar, M.A. and Azadegan Dehkordi, F. and Farrokhi, E. and Akbari, M.T. and Hashemzade Chaleshtori, M. (2012) Large-Scale Screening of Mitochondrial DNA Mutations Among Iranian Patients with Prelingual Nonsyndromic Hearing Impairment. GENETIC TESTING AND MOLECULAR BIOMARKERS, 16 (4). pp. 271-278.

Ahani, A. and Khoramkhorshid, H. and Behnam, B. and Akbari, M.T. (2012) Report of a novel mutation in Rb1 gene from an Iranian retinoblastoma patient and its effect on splicing pattern of mRNA. Journal of Shahrekord Uuniversity of Medical Sciences, 14.

Teimori, H. and Akbari, M.T. and Hamid, M. and Forouzandeh, M. and Bibordi, E. (2011) Analysis of CD38 and ZAP70 mRNA expression among cytogenetic subgroups of Iranian chronic-lymphocytic-leukemia patients. GENETICS AND MOLECULAR RESEARCH, 10 (4). pp. 2415-2423.

Hashmzade Chaleshtori, M. and Akbari, M.T. and Khazraei, H. and Abolhasani, M. and Reisi, S. and Ataei, Z. and Saedi-Marghmaleki, M. and Shirmardi, S.A. and Farrokhi,, E. and Montazer-Zohouri, M. and Azadegan-Dehkordi, F. (2011) Screening of three common mtDNA mutations among subjects with autosomal recessive non-syndromic hearing loss in Sistan va Baluchestan province, Iran. Zahedan Journal of Research in Medical Sciences, 13 (5).

Teimori, H. and Akbari, M.T. and Toogeh, GR. and Khaleghian, M. (2010) Correlation of del13q, del11q and Trisomy 12 with Laboratory and Clinical Features of Chronic Lymphocytic Leukemia in Iranian Patients. Iranian Red Crescent Medical Journal, 12 (5).

Hamidi, M. and Karimipoor, M. and Hashemzadeh Chaleshtori, M. and Akbari, M.T. (2009) A novel 355-357delGAG mutation and frequency of connexin-26 (GJB2) mutations in Iranian patients. JOURNAL OF GENETICS, 88 (3). pp. 359-362.

This list was generated on Fri Nov 24 01:09:56 2017 IRST.