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Year | Number of Results |
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2008 | 1 |
2014 | 1 |
2015 | 1 |
2024 | 1 |
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Clinical application of next generation sequencing for Mendelian disease diagnosis in the Iranian population.
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.
Eight novel mutations in MLC1 from 18 Iranian patients with megalencephalic leukoencephalopathy with subcortical cysts.
Kariminejad A, Rajaee A, Ashrafi MR, Alizadeh H, Tonekaboni SH, Malamiri RA, Ghofrani M, Karimzadeh P, Mohammadi MM, Baghalshooshtari A, Bozorgmehr B, Kariminejad MH, Postma N, Abbink TE, van der Knaap MS.
Kariminejad A, et al.
Eur J Med Genet. 2015 Feb;58(2):71-4. doi: 10.1016/j.ejmg.2014.12.004. Epub 2014 Dec 11.
Eur J Med Genet. 2015.
PMID: 25497041
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Skull defects, alopecia and distinctive facies: a new syndrome?
Kariminejad A, Bozorgmehr B, Ashrafi MR, Kariminejad MH.
Kariminejad A, et al.
Clin Dysmorphol. 2008 Jul;17(3):203-205. doi: 10.1097/MCD.0b013e3282fba59d.
Clin Dysmorphol. 2008.
PMID: 18541970
No abstract available.
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