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Genetic Analysis of MECP2 Gene in Iranian Patients with Rett Syndrome.
Iran J Child Neurol. 2019 Summer;13(3):25-34.
Iran J Child Neurol. 2019.
PMID: 31327966
Free PMC article.
Detection of intragenic SMN1 mutations in spinal muscular atrophy patients with a single copy of SMN1.
Ganji H, Nouri N, Salehi M, Aryani O, Houshmand M, Basiri K, Fazel-Najafabadi E, Sedghi M.
Ganji H, et al. Among authors: fazel najafabadi e.
J Child Neurol. 2015 Apr;30(5):558-62. doi: 10.1177/0883073814521297. Epub 2014 Feb 20.
J Child Neurol. 2015.
PMID: 24563475
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Evaluation of multiplex ligation-dependent probe amplification analysis versus multiplex polymerase chain reaction assays in the detection of dystrophin gene rearrangements in an Iranian population subset.
Nouri N, Fazel-Najafabadi E, Salehi M, Hosseinzadeh M, Behnam M, Ghazavi MR, Sedghi M.
Nouri N, et al. Among authors: fazel najafabadi e.
Adv Biomed Res. 2014 Jan 27;3:72. doi: 10.4103/2277-9175.125862. eCollection 2014.
Adv Biomed Res. 2014.
PMID: 24627880
Free PMC article.
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A new compound heterozygous mutation in GJB2 causes nonsyndromic hearing loss in a consanguineous Iranian family.
Keivani A, Haghighat-Nia A, Fazel-Najafabadi E, Hosseinzadeh M, Salehi M.
Keivani A, et al. Among authors: fazel najafabadi e.
Int J Pediatr Otorhinolaryngol. 2015 Apr;79(4):553-6. doi: 10.1016/j.ijporl.2015.01.027. Epub 2015 Jan 30.
Int J Pediatr Otorhinolaryngol. 2015.
PMID: 25708704
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Use of in silico tools for classification of novel missense mutations identified in dystrophin gene in developing countries.
Nouri N, Fazel-Najafabadi E, Behnam M, Nouri N, Aryani O, Ghasemi M, Nasiri J, Sedghi M.
Nouri N, et al. Among authors: fazel najafabadi e.
Gene. 2014 Feb 10;535(2):250-4. doi: 10.1016/j.gene.2013.11.022. Epub 2013 Nov 22.
Gene. 2014.
PMID: 24274981
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Mutation spectrum of autosomal recessive non-syndromic hearing loss in central Iran.
Haghighat-Nia A, Keivani A, Nadeali Z, Fazel-Najafabadi E, Hosseinzadeh M, Salehi M.
Haghighat-Nia A, et al. Among authors: fazel najafabadi e.
Int J Pediatr Otorhinolaryngol. 2015 Nov;79(11):1892-5. doi: 10.1016/j.ijporl.2015.08.039. Epub 2015 Sep 2.
Int J Pediatr Otorhinolaryngol. 2015.
PMID: 26409293
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Structural and functional impact of missense mutations in TPMT: An integrated computational approach.
Fazel-Najafabadi E, Vahdat Ahar E, Fattahpour S, Sedghi M.
Fazel-Najafabadi E, et al.
Comput Biol Chem. 2015 Dec;59 Pt A:48-55. doi: 10.1016/j.compbiolchem.2015.09.004. Epub 2015 Sep 9.
Comput Biol Chem. 2015.
PMID: 26410243
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Genomic rearrangement screening of the BRCA1 from seventy Iranian high-risk breast cancer families.
Sedghi M, Esfandiari E, Fazel-Najafabadi E, Salehi M, Salavaty A, Fattahpour S, Dehghani L, Nouri N, Mokarian F.
Sedghi M, et al. Among authors: fazel najafabadi e.
J Res Med Sci. 2016 Nov 2;21:95. doi: 10.4103/1735-1995.193167. eCollection 2016.
J Res Med Sci. 2016.
PMID: 28163741
Free PMC article.
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