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Page 1
Comprehensive copy number analysis of spinal muscular atrophy among the Iranian population.
Khanbazi A, Beheshtian M, Azad M, Akbari Kelishomi M, Afroozan F, Fatehi F, Noudehi K, Zamanian Najafabadi S, Omrani M, Habibi H, Taghdiri M, Abdi Rad I, Nafissi S, Jankhah A, Yazdan H, Daneshmand P, Saberi SH, Kahrizi K, Kariminejad A, Najmabadi H. Khanbazi A, et al. Among authors: yazdan h. Sci Rep. 2024 Dec 2;14(1):29880. doi: 10.1038/s41598-024-76815-x. Sci Rep. 2024. PMID: 39622884 Free PMC article.
Clinical application of next generation sequencing for Mendelian disease diagnosis in the Iranian population.
Abolhassani A, Fattahi Z, Beheshtian M, Fadaee M, Vazehan R, Ahangari F, Dehdahsi S, Faraji Zonooz M, Parsimehr E, Kalhor Z, Peymani F, Mozaffarpour Nouri M, Babanejad M, Noudehi K, Fatehi F, Zamanian Najafabadi S, Afroozan F, Yazdan H, Bozorgmehr B, Azarkeivan A, Sadat Mahdavi S, Nikuei P, Fatehi F, Jamali P, Ashrafi MR, Karimzadeh P, Habibi H, Kahrizi K, Nafissi S, Kariminejad A, Najmabadi H. Abolhassani A, et al. Among authors: yazdan h. NPJ Genom Med. 2024 Feb 19;9(1):12. doi: 10.1038/s41525-024-00393-0. NPJ Genom Med. 2024. PMID: 38374194 Free PMC article.
The spectrum of GJB2 mutations in the Iranian population with non-syndromic hearing loss--a twelve year study.
Bazazzadegan N, Nikzat N, Fattahi Z, Nishimura C, Meyer N, Sahraian S, Jamali P, Babanejad M, Kashef A, Yazdan H, Sabbagh Kermani F, Taghdiri M, Azadeh B, Mojahedi F, Khoshaeen A, Habibi H, Reyhanifar F, Nouri N, Smith RJ, Kahrizi K, Najmabadi H. Bazazzadegan N, et al. Among authors: yazdan h. Int J Pediatr Otorhinolaryngol. 2012 Aug;76(8):1164-74. doi: 10.1016/j.ijporl.2012.04.026. Epub 2012 Jun 12. Int J Pediatr Otorhinolaryngol. 2012. PMID: 22695344
The frequency of GJB2 mutations and the Delta (GJB6-D13S1830) deletion as a cause of autosomal recessive non-syndromic deafness in the Kurdish population.
Mahdieh N, Nishimura C, Ali-Madadi K, Riazalhosseini Y, Yazdan H, Arzhangi S, Jalalvand K, Ebrahimi A, Kazemi S, Smith RJ, Najmabadi H. Mahdieh N, et al. Among authors: yazdan h. Clin Genet. 2004 Jun;65(6):506-8. doi: 10.1111/j.1399-0004.2004.00262.x. Clin Genet. 2004. PMID: 15151513 No abstract available.