Related references
Note: Only part of the references are listed.ANTERIOR CHAMBER DEPTH AND PRIMARY ANGLE-CLOSURE GLAUCOMA
P. H. ALSBIRK
ACTA OPHTHALMOLOGICA (2009)
Glaucoma in aniridia
D. Bremond-Gignac
JOURNAL FRANCAIS D OPHTALMOLOGIE (2007)
A novel mutation in the DNA-binding domain of MAF at 16q23.1 associated with autosomal dominant cerulean cataract in an Indian family
V Vanita et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2006)
The number of people with glaucoma worldwide in 2010 and 2020
HA Quigley et al.
BRITISH JOURNAL OF OPHTHALMOLOGY (2006)
Developmental malformations of the eye: the role of PAX6, SOX2 and OTX2
A. M. Hever et al.
CLINICAL GENETICS (2006)
Extreme hyperopia is the result of null mutations in MFRP, which encodes a Frizzled-related protein
OH Sundin et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)
Anterior chamber depth and the risk of primary angle closure in 2 East Asian populations
T Aung et al.
ARCHIVES OF OPHTHALMOLOGY (2005)
Molecular gradients and development of retinotopic maps
T McLaughlin et al.
ANNUAL REVIEW OF NEUROSCIENCE (2005)
Mutations of VMD2 splicing regulators cause nanophthalmos and autosomal dominant vitreoretinochoroidopathy (ADVIRC)
J Yardley et al.
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE (2004)
Anterior segment development relevant to glaucoma
DB Gould et al.
INTERNATIONAL JOURNAL OF DEVELOPMENTAL BIOLOGY (2004)
A locus for autosomal dominant colobomatous microphthalmia maps to chromosome 15q12-q15
L Morlé et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2000)
Rom-1 is required for rod photoreceptor viability and the regulation of disk morphogenesis
G Clarke et al.
NATURE GENETICS (2000)