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Firasat S 1

Showing records 1 to 1 | Display all abstracts from Firasat S

69968 A spectrum of CYP1B1 mutations associated with primary congenital glaucoma in families of Pakistani descent
Rauf B; Irum B; Kabir F; Firasat S; Naeem MA; Khan SN; Husnain T; Riazuddin S; Akram J; Riazuddin SA
Human genome variation 2016; 3: 16021

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