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Page 1
The Iranian human mutation database.
Motazacker MM, Taherzadeh-Fard E, Husseini Z, Behjati F, Esteghamat F, Kahrizi K, Najmabadi H. Motazacker MM, et al. Among authors: esteghamat f. Arch Iran Med. 2007 Jul;10(3):372-5. Arch Iran Med. 2007. PMID: 17604476 No abstract available.
Screening for MYO15A gene mutations in autosomal recessive nonsyndromic, GJB2 negative Iranian deaf population.
Fattahi Z, Shearer AE, Babanejad M, Bazazzadegan N, Almadani SN, Nikzat N, Jalalvand K, Arzhangi S, Esteghamat F, Abtahi R, Azadeh B, Smith RJ, Kahrizi K, Najmabadi H. Fattahi Z, et al. Among authors: esteghamat f. Am J Med Genet A. 2012 Aug;158A(8):1857-64. doi: 10.1002/ajmg.a.34411. Epub 2012 Jun 26. Am J Med Genet A. 2012. PMID: 22736430 Free PMC article.
Did the GJB2 35delG mutation originate in Iran?
Norouzi V, Azizi H, Fattahi Z, Esteghamat F, Bazazzadegan N, Nishimura C, Nikzat N, Jalalvand K, Kahrizi K, Smith RJ, Najmabadi H. Norouzi V, et al. Among authors: esteghamat f. Am J Med Genet A. 2011 Oct;155A(10):2453-8. doi: 10.1002/ajmg.a.34225. Epub 2011 Sep 9. Am J Med Genet A. 2011. PMID: 21910243 Free PMC article.
Molecular mechanisms underlying thalassemia intermedia in Iran.
Neishabury M, Azarkeivan A, Oberkanins C, Esteghamat F, Amirizadeh N, Najmabadi H. Neishabury M, et al. Among authors: esteghamat f. Genet Test. 2008 Dec;12(4):549-56. doi: 10.1089/gte.2008.0018. Genet Test. 2008. PMID: 18939939
A report of 8 cases with hemoglobin H disease in an Iranian family.
Azarkeivan A, Neishabury M, Hadavi V, Esteghamat F, Enrahimkhani S, Najmabadi H. Azarkeivan A, et al. Among authors: esteghamat f. Pediatr Hematol Oncol. 2010 Aug;27(5):405-12. doi: 10.3109/08880010903536201. Pediatr Hematol Oncol. 2010. PMID: 20670167
Hydroxyurea responsiveness in β-thalassemic patients is determined by the stress response adaptation of erythroid progenitors and their differentiation propensity.
Pourfarzad F, von Lindern M, Azarkeivan A, Hou J, Kia SK, Esteghamat F, van Ijcken W, Philipsen S, Najmabadi H, Grosveld F. Pourfarzad F, et al. Among authors: esteghamat f. Haematologica. 2013 May;98(5):696-704. doi: 10.3324/haematol.2012.074492. Epub 2012 Oct 25. Haematologica. 2013. PMID: 23100274 Free PMC article.
Two novel GALNT3 mutations in familial tumoral calcinosis.
Garringer HJ, Mortazavi SM, Esteghamat F, Malekpour M, Boztepe H, Tanakol R, Davis SI, White KE. Garringer HJ, et al. Among authors: esteghamat f. Am J Med Genet A. 2007 Oct 15;143A(20):2390-6. doi: 10.1002/ajmg.a.31947. Am J Med Genet A. 2007. PMID: 17853462
Erythropoiesis and globin switching in compound Klf1::Bcl11a mutant mice.
Esteghamat F, Gillemans N, Bilic I, van den Akker E, Cantù I, van Gent T, Klingmüller U, van Lom K, von Lindern M, Grosveld F, Bryn van Dijk T, Busslinger M, Philipsen S. Esteghamat F, et al. Blood. 2013 Mar 28;121(13):2553-62. doi: 10.1182/blood-2012-06-434530. Epub 2013 Jan 29. Blood. 2013. PMID: 23361909 Free article.
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