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Paylakhi SH 2

Showing records 1 to 2 | Display all abstracts from Paylakhi SH

24610 Loss of function mutations in the gene encoding latent transforming growth factor beta binding protein 2, LTBP2, cause primary congenital glaucoma
Narooie-Nejad M; Paylakhi SH; Shojaee S; Fazlali Z; Rezaei Kanavi M; Nilforushan N; Yazdani S; Babrzadeh F; Suri F; Ronaghi M
Human Molecular Genetics 2009; 18: 3969-3977

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24966 Variable expressivity and high penetrance of CYP1B1 mutations associated with primary congenital glaucoma
Suri F; Yazdani S; Narooie-Nejhad M; Zargar SJ; Paylakhi SH; Zeinali S; Pakravan M; Elahi E
Ophthalmology 2009; 116: 2101-2109

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