advertisement
Husnain T 1
Showing records 1 to 1 | Display all abstracts from Husnain T69968 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
