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Burdon KP 2

Showing records 1 to 2 | Display all abstracts from Burdon KP

47828 The association of hepatocyte growth factor (HGF) gene with primary angle closure glaucoma in the Nepalese population
Awadalla MS; Thapa SS; Burdon KP; Hewitt AW; Craig JE
Molecular Vision 2011; 17: 2248-2254

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47503 Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucoma
Khan K; Rudkin A; Parry DA; Burdon KP; McKibbin M; Logan CV; Abdelhamed ZIA; Muecke JS; Fernandez-Fuentes N; Laurie KJ
American Journal of Human Genetics 2011; 89: 464-473

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