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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
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
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
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
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
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