William H. Murphey

Genetic heterogeneity among blue-cone monochromats.

J. Nathans, L. Sharpe, E. Zrenner, 1993, American journal of human genetics.

Autosomal dominant congenital cataract associated with a missense mutation in the human alpha crystallin gene CRYAA.

P. Kramer, R. Weleber, M. Litt, 1998, Human molecular genetics.

Characterization of the ocular phenotype of Duchenne and Becker muscular dystrophy.

C. Westall, P. Ray, B. Powell, 1994, Ophthalmology.