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Nilforooshan N 1
Showing records 1 to 1 | Display all abstracts from Nilforooshan N19818 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; Zare Mehrjerdi MA
Journal of Molecular Diagnostics 2007; 9: 382-393
