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Identification of rare hemoglobin variant (Hb Fairfax) causing dominant β-thalassemia phenotype in an Iranian family.

Mohammad Taghi Akbari , Mohammad Hamid , Mina Izadyar
Annals of Hematology, 2011, 90 (3), pp.349-51. ⟨10.1007/s00277-010-1003-4⟩
Journal articles istex pasteur-00750569v1
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Clinical features, DYT1 mutation screening and genotype-phenotype correlation in patients with dystonia from Iran.

Mohammad Hamid , Mohammad Taghi Akbari , Gholam Ali Shahidi , Zahra Zand
Medical Principles and Practice, 2012, 21 (5), pp.462-6. ⟨10.1159/000336783⟩
Journal articles pasteur-00753523v1
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Analysis of CD38 and ZAP70 mRNA expression among cytogenetic subgroups of Iranian chronic-lymphocytic-leukemia patients.

H. Teimori , M. T. Akbari , M. Hamid , M. Forouzandeh , E. Bibordi
Genetics and molecular research : GMR, 2011, 10 (4), pp.2415-23. ⟨10.4238/2011.October.7.3⟩
Journal articles pasteur-00751231v1
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Identification of α-globin chain variants: a report from Iran.

Mohammad Taghi Akbari , Mohammad Hamid
Archives of Iranian Medicine, 2012, 15 (9), pp.564-567
Journal articles pasteur-00750568v1
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The Cretan type of nondeletional hereditary persistence of fetal hemoglobin in an Iranian family.

Mohammad Hamid , Frouzandeh Mahjoubi , Mohammad Taghi Akbari , Sirous Zeinali , Morteza Karimipoor
Annals of Hematology, 2009, 88 (12), pp.1267-8. ⟨10.1007/s00277-009-0756-0⟩
Journal articles istex pasteur-00751227v1
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Transient expression assay of Agamma-588 (A/G) mutations in the K562 cell line.

Mohammad Hamid , Frouzandeh Mahjoubi , Mohammad Taghi Akbari , Hossein Khanahmad , Fatemeh Jamshidi , et al.
Iranian Biomedical Journal, 2011, 15 (1-2), pp.15-21
Journal articles pasteur-00746421v1