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A haplotype framework for cystic fibrosis mutations in Iran.
Elahi E, Khodadad A, Kupershmidt I, Ghasemi F, Alinasab B, Naghizadeh R, Eason RG, Amini M, Esmaili M, Esmaeili Dooki MR, Sanati MH, Davis RW, Ronaghi M, Thorstenson YR. Elahi E, et al. Among authors: sanati mh. J Mol Diagn. 2006 Feb;8(1):119-27. doi: 10.2353/jmoldx.2006.050063. J Mol Diagn. 2006. PMID: 16436643 Free PMC article.
Contributions of MYOC and CYP1B1 mutations to JOAG.
Bayat B, Yazdani S, Alavi A, Chiani M, Chitsazian F, Tusi BK, Suri F, Narooie-Nejhad M, Sanati MH, Elahi E. Bayat B, et al. Among authors: sanati mh. Mol Vis. 2008 Mar 13;14:508-17. Mol Vis. 2008. PMID: 18385784 Free PMC article.
CYP1B1 mutation profile of Iranian primary congenital glaucoma patients and associated haplotypes.
Chitsazian F, Tusi BK, Elahi E, Saroei HA, Sanati MH, Yazdani S, Pakravan M, Nilforooshan N, Eslami Y, Mehrjerdi MA, Zareei R, Jabbarvand M, Abdolahi A, Lasheyee AR, Etemadi A, Bayat B, Sadeghi M, Banoei MM, Ghafarzadeh B, Rohani MR, Rismanchian A, Thorstenson Y, Sarfarazi M. Chitsazian F, et al. Among authors: sanati mh. J Mol Diagn. 2007 Jul;9(3):382-93. doi: 10.2353/jmoldx.2007.060157. J Mol Diagn. 2007. PMID: 17591938 Free PMC article.
169 results