S. Xu

Homozygosity mapping of autosomal recessive retinitis pigmentosa locus (RP22) on chromosome 16p12.1-p12.3.

J. Weber, U. Finckh, A. Gal, 1998, Genomics.

Gene for autosomal dominant congenital stationary night blindness maps to the same region as the gene for the beta-subunit of the rod photoreceptor cGMP phosphodiesterase (PDEB) in chromosome 4p16.3.

T. Rosenberg, H. Eiberg, E. Schwinger, 1994, Human molecular genetics.

Variable expressivity in a Japanese family with autosomal dominant retinitis pigmentosa closely linked to chromosome 19q.

M. Tamai, A. Gal, M. Nakazawa, 1996, Archives of ophthalmology.

Autosomal dominant retinitis pigmentosa locus on chromosome 19q in a Japanese family.

M. Tamai, A. Gal, M. Nakazawa, 1995, Journal of medical genetics.

A ninth locus (RP18) for autosomal dominant retinitis pigmentosa maps in the pericentromeric region of chromosome 1.

T. Rosenberg, M. Schwartz, A. Gal, 1996, Human molecular genetics.

A missense point mutation (Leu13Arg) of the Norrie disease gene in a large Cuban kindred with Norrie disease.

M. Salcedo, A. Gal, H. Wedemann, 1994, Human molecular genetics.