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Year | Number of Results |
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2013 | 1 |
2014 | 4 |
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7 results
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Page 1
Causative variants linked with limb girdle muscular dystrophy in an Iranian population: 6 novel variants.
Mol Genet Genomic Med. 2023 Feb;11(2):e2101. doi: 10.1002/mgg3.2101. Epub 2022 Nov 14.
Mol Genet Genomic Med. 2023.
PMID: 36374152
Free PMC article.
Association of AHSG with alopecia and mental retardation (APMR) syndrome.
Reza Sailani M, Jahanbani F, Nasiri J, Behnam M, Salehi M, Sedghi M, Hoseinzadeh M, Takahashi S, Zia A, Gruber J, Lynch JL, Lam D, Winkelmann J, Amirkiai S, Pang B, Rego S, Mazroui S, Bernstein JA, Snyder MP.
Reza Sailani M, et al.
Hum Genet. 2017 Mar;136(3):287-296. doi: 10.1007/s00439-016-1756-5. Epub 2017 Jan 4.
Hum Genet. 2017.
PMID: 28054173
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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.
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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Homozygous MAPT R406W mutation causing FTDP phenotype: A unique instance of a unique mutation.
Behnam M, Ghorbani F, Shin JH, Kim DS, Jang H, Nouri N, Sedghi M, Salehi M, Ansari B, Basiri K.
Behnam M, et al.
Gene. 2015 Oct 1;570(1):150-2. doi: 10.1016/j.gene.2015.06.033. Epub 2015 Jun 15.
Gene. 2015.
PMID: 26086902
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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.
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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Genotype-phenotype correlation of survival motor neuron and neuronal apoptosis inhibitory protein genes in spinal muscular atrophy patients from Iran.
Sedghi M, Behnam M, Fazel E, Salehi M, Ganji H, Meamar R, Hosseinzadeh M, Nouri N.
Sedghi M, et al.
Adv Biomed Res. 2014 Jan 27;3:74. doi: 10.4103/2277-9175.125872. eCollection 2014.
Adv Biomed Res. 2014.
PMID: 24627882
Free PMC article.
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A novel missense mutation in the GNE gene in an Iranian patient with hereditary inclusion body myopathy.
Behnam M, Jin-Hong S, Kim DS, Basiri K, Nilipour Y, Sedghi M.
Behnam M, et al.
J Res Med Sci. 2014 Aug;19(8):792-4.
J Res Med Sci. 2014.
PMID: 25422667
Free PMC article.
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