L. Beck

Cataract and myotonic dystrophy: the role of molecular diagnosis.

W. Reardon, D. Shaw, P. Harper, 1993, The British journal of ophthalmology.

Photoscreening for refractive errors in children and young adults with severe learning disabilities using the MTI photoscreener

L. Beck, P. Watts, K. Walker, 1999, Eye.

Adrenal suppression and failure to thrive after steroid injections for periocular hemangioma.

J. Gregory, L. Beck, P. Watts, 2004, Ophthalmology.

Goldenhar and cri-du-chat syndromes: a contiguous gene deletion syndrome?

Y. Choong, L. Beck, P. Watts, 2003, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

Phenotypic evidence for a common pathogenesis in X-linked deafness pedigrees and in Xq13-q21 deletion related deafness.

W. Reardon, N. S. Thomas, P. Phelps, 1992, American journal of medical genetics.

Dysthyroid eye disease presenting as Brown's syndrome

L. Beck, R. Hill, D. Hughes, 1993, Acta ophthalmologica.

Linkage analysis in an autosomal dominant ‘zonular nuclear pulverulent’ congenital cataract, mapped to chromosome 13q11-13

M. Owen, A. Clarke, M. Rees, 2000, Eye.

Latanoprost, a prostaglandin analog, for glaucoma therapy. Efficacy and safety after 1 year of treatment in 198 patients. Latanoprost Study Groups.

R. Schumer, R. Ritch, D. Steinberger, 1996, Ophthalmology.