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American Journal of Ophthalmology|April 9, 2001
The Taa1 restriction enzyme provides a simple means to identify the Q368STOP mutation of the myocilin gene in primary open angle glaucomaP N Baird, J Dickinson, J E Craig, et al.
Human Molecular Genetics|August 1, 1992
Constitutional mutations in the WT1 gene in patients with Denys-Drash syndromeP N Baird, A Santos, N Groves, et al.
Ophthalmic Research|March 27, 2009
Role of genetic factors in lower- and higher-order aberrations--the genes in myopia twin studyM Dirani, M Chamberlain, T A Couper, et al.
Oncogene|November 1, 1992
Identification of mutations in the WT1 gene in tumours from patients with the WAGR syndromeP N Baird, N Groves, D A Haber, et al.
Ophthalmic Epidemiology|June 24, 2008
Testing protocol and recruitment in the genes in myopia twin studyM Dirani, M Chamberlain, P Garoufalis, et al.
The British Journal of Ophthalmology|November 21, 2008
The dot-and-fleck retinopathy of X linked Alport syndrome is independent of complement factor H (CFH) gene polymorphismsJ Liu, D Colville, Y Y Wang, et al.
Human Genetics|August 1, 1993
Insertional inactivation of the WT1 gene in tumour cells from a patient with WAGR syndromeA Santos, L Osorio-Almeida, P N Baird, et al.
Eye (London, England)|June 30, 2012
Heritability of the spatial distribution and peak density of macular pigment: a classical twin studyR E Hogg, E L Ong, M Chamberlain, et al.
Vision Research|February 21, 2002
Generating mouse models of retinal disease using ENU mutagenesisP N Baird, R H Guymer, D Chiu, et al.
Molecular Vision|July 24, 2009
The retinoic acid receptor alpha (RARA) gene is not associated with myopia, hypermetropia, and ocular biometric measuresS Veerappan, M Schäche, K K Pertile, et al.
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