Mohammad Ali Dowlati - Search Results

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Year	Number of Results
2012	3
2013	3
2025	0

Page 1

Novel nucleotide changes in mutational analysis of mitochondrial 12SrRNA gene in patients with nonsyndromic and aminoglycoside-induced hearing loss.

Dowlati MA, Derakhshandeh-Peykar P, Houshmand M, Farhadi M, Shojaei A, Fallah M, Mohammadi E, Tajdini A, Arastoo S, Tavakkoly-Bazzaz J. Dowlati MA, et al. Mol Biol Rep. 2013 Mar;40(3):2689-95. doi: 10.1007/s11033-012-2355-8. Epub 2012 Dec 16. Mol Biol Rep. 2013. PMID: 23242658

Partial trisomy 7q and monosomy 13q in a child with disorder of sex development: phenotypic and genotypic findings.

Shojaei A, Behjati F, Derakhshandeh-Peykar P, Razzaghy-Azar M, Otukesh H, Kariminejad R, Dowlati MA, Rashidi-Nezhad A, Tavakkoly-Bazzaz J. Shojaei A, et al. Among authors: dowlati ma. Gene. 2013 Mar 15;517(1):137-45. doi: 10.1016/j.gene.2012.11.013. Epub 2012 Nov 30. Gene. 2013. PMID: 23201896

Novel human mitochondrial tRNA phe mutation in a patient with hearing impairment: a case study.

Dowlati MA, Derakhshandeh-Peykar P, Houshmand M, Farhadi M, Shojaei A, Bazzaz JT. Dowlati MA, et al. Mitochondrial DNA. 2013 Apr;24(2):132-6. doi: 10.3109/19401736.2012.717935. Epub 2012 Sep 14. Mitochondrial DNA. 2013. PMID: 22979943

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