Close linkage between Norrie disease, a cloned DNA sequence from the proximal short arm, and the centromere of the X chromosomeBLEEKER-WAGEMAKERS, L. M; FRIEDRICH, U; GAL, A et al.Human genetics. 1985, Vol 71, Num 3, pp 211-214, issn 0340-6717Article

Refinement of the chromosomal position of the X linked juvenile retinoschisis geneBERGEN, A. A. B; GEN BRINK, J. B; BLEEKER-WAGEMAKERS, L. M et al.Journal of medical genetics. 1994, Vol 31, Num 12, pp 972-975, issn 0022-2593Article

Oculocerebrocutaneous syndromeBLEEKER-WAGEMAKERS, L. M; HAMEL, B. C. J; HENNEKAM, R. C. M et al.Journal of medical genetics. 1990, Vol 27, Num 1, pp 69-70, issn 0022-2593, 2 p.Article

Assignment of a gene for autosomal recessive retinitis pigmentosa (RP12) to chromosome 1q31-q32.1 in an inbred and genetically heterogeneous disease populationVAN SOEST, S; VAN DEN BORN, L. I; GAL, A et al.Genomics (San Diego, Calif.). 1994, Vol 22, Num 3, pp 499-504, issn 0888-7543Article

Evidence for nonallelic genetic heterogeneity in autosomal recessive retinitis pigmentosaBLEEKER-WAGEMAKERS, L. M; GAL, A; FARRAR, G. J et al.Genomics (San Diego, Calif.). 1992, Vol 14, Num 3, pp 811-812, issn 0888-7543Article

Positional cloning of the gene for X-linked retinitis pigmentosa 3 : homology with the guanine-nucleotide-exchange factor RCC1ROEPMAN, R; VAN DUIJNHOVEN, G; CREMERS, F. P. M et al.Human molecular genetics (Print). 1996, Vol 5, Num 7, pp 1035-1042, issn 0964-6906, 7 p.Article

Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on XpGAL, A; SCHINZEL, A; ORTH, U et al.Human genetics. 1989, Vol 81, Num 4, pp 315-318, issn 0340-6717Article