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Primary congenital glaucoma caused by the homozygous F261L CYP1B1 mutation and paternal isodisomy of chromosome 2

✍ Scribed by M-P López-Garrido; E Campos-Mollo; M-Á Harto; J Escribano


Book ID
110888855
Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
585 KB
Volume
76
Category
Article
ISSN
0009-9163

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