Salehi M - Search Results

1

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: salehi m. 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

2

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: salehi m. J Child Neurol. 2015 Apr;30(5):558-62. doi: 10.1177/0883073814521297. Epub 2014 Feb 20. J Child Neurol. 2015. PMID: 24563475

3

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: salehi m. 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.

4

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. Among authors: salehi m. 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.

5

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: salehi m. 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

6

Identification of Proximal and Distal 22q11.2 Microduplications among Patients with Cleft Lip and/or Palate: A Novel Inherited Atypical 0.6 Mb Duplication.

Sedghi M, Abdali H, Memarzadeh M, Salehi M, Nouri N, Hosseinzadeh M, Nouri N. Sedghi M, et al. Among authors: salehi m. Genet Res Int. 2015;2015:398063. doi: 10.1155/2015/398063. Epub 2015 Nov 12. Genet Res Int. 2015. PMID: 26640714 Free PMC article.

7

Reciprocal 22q11.2 Deletion and Duplication in Siblings with Karyotypically Normal Parents.

Demaerel W, Hosseinzadeh M, Nouri N, Sedghi M, Dimitriadou E, Salehi M, Abdali H, Memarzadeh M, Zamani M, Vermeesch JR. Demaerel W, et al. Among authors: salehi m. Cytogenet Genome Res. 2016;148(1):1-5. doi: 10.1159/000445089. Epub 2016 Apr 8. Cytogenet Genome Res. 2016. PMID: 27055209

8

Investigation of TBX1 gene deletion in Iranian children with 22q11.2 deletion syndrome: correlation with conotruncal heart defects.

Ganji H, Salehi M, Sedghi M, Abdali H, Nouri N, Sadri L, Hosseinzadeh M, Vakili B, Lotfi M. Ganji H, et al. Among authors: salehi m. Heart Asia. 2013 Sep 12;5(1):200-2. doi: 10.1136/heartasia-2013-010327. eCollection 2013. Heart Asia. 2013. PMID: 27326128 Free PMC article.

9

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: salehi m. 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.

10

A novel homozygous DPH1 mutation causes intellectual disability and unique craniofacial features.

Sekiguchi F, Nasiri J, Sedghi M, Salehi M, Hosseinzadeh M, Okamoto N, Mizuguchi T, Nakashima M, Miyatake S, Takata A, Miyake N, Matsumoto N. Sekiguchi F, et al. Among authors: salehi m. J Hum Genet. 2018 Apr;63(4):487-491. doi: 10.1038/s10038-017-0404-9. Epub 2018 Feb 6. J Hum Genet. 2018. PMID: 29410513

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

1,513 results

Search Page

Filters