Identification of a key recombinant which assigns the incomplete congenital stationary night blindness gene proximal to MAOBBERGEN, A. A. B; KESTELYN, P; LEYS, M et al.Journal of medical genetics. 1994, Vol 31, Num 7, pp 580-582, issn 0022-2593Article

Localization of a novel X-linked progressive cone dystrophy gene to Xq27 : Evidence for genetic heterogeneityBERGEN, A. A. B; PINCKERS, A. J. L. G.American journal of human genetics. 1997, Vol 60, Num 6, pp 1468-1473, issn 0002-9297Article

Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCRCREMERS, F. P. M; VAN DE POL, D. J. R; PINCKERS, A. J. L. G et al.Human molecular genetics (Print). 1998, Vol 7, Num 3, pp 355-362, issn 0964-6906Article

Efficient DNA carrier detection in X linked juvenile retinoschisisBERGEN, A. A. B; TEN BRINK, J. B; VAN SCHOONEVELD, M. J et al.British journal of ophthalmology. 1995, Vol 79, Num 7, pp 683-686, issn 0007-1161Article

What are the mechanisms of photoreceptor adaptation ?BOWNDS, M. D; ARSHAVSKY, V. Y.Behavioral and brain sciences (Print). 1995, Vol 18, Num 3, pp 415-424, issn 0140-525XArticle

Recoverin and Ca²⁺ in vertebrate phototransductionHURLEY, J. B.Behavioral and brain sciences (Print). 1995, Vol 18, Num 3, pp 425-428, issn 0140-525XArticle

Controversies in neuroscience III : Signal transduction in the retina. Commentaries. Authors' repliesABRAMS, T. W; ALBERT, A. D; GARAVITO, R. M et al.Behavioral and brain sciences (Print). 1995, Vol 18, Num 3, pp 468-521, issn 0140-525XSerial Issue

Detection of a new submicroscopic Norrie disease deletion interval with a novel DNA probe isolated by differential Alu PCR fingerprint cloningBERGEN, A. A. B; WAPENAAR, M. C; SCHUURMAN, E. J. M et al.Cytogenetics and cell genetics. 1993, Vol 62, Num 4, pp 231-235, issn 0301-0171Article

Pseudoxanthoma elasticum maps to an 820-kb region of the p13.1 region of chromosome 16LE SAUX, O; URBAN, Z; BREUNING, M et al.Genomics (San Diego, Calif.). 1999, Vol 62, Num 1, pp 1-10, issn 0888-7543Article

Identification of the gene responsible for Best macular dystrophyPETRUKHIN, K; KOISTI, M. J; VUJIC, M et al.Nature genetics. 1998, Vol 19, Num 3, pp 241-247, issn 1061-4036Article

Characterization of SCML1, a new gene in Xp22, with homology to developmental polycomb genesVAN DE VOSSE, E; WALPOLE, S. M; GRAFHAM, D et al.Genomics (San Diego, Calif.). 1998, Vol 49, Num 1, pp 96-102, issn 0888-7543Article

The cGMP-gated channel of photoreceptor cells : its structural properties and role in phototransductionMOLDAY, R. S; HSU, Y.-T.Behavioral and brain sciences (Print). 1995, Vol 18, Num 3, pp 441-451, issn 0140-525XArticle

A submicroscopic deletion in a patient with isolated X-linked ocular albinism (OA1)BASSI, M. T; BERGEN, A. A. B; WAPENAAR, M. C et al.Human molecular genetics (Print). 1994, Vol 3, Num 4, pp 647-648, issn 0964-6906Article

Integrated genetic and physical map of the 1q31 → q32.1 region, encompassing the RP12 locus, the F13B and HF1 genes, and the EEF1AL11 and RPL30 pseudogenesVAN SOEST, S; VAN ROSSEM, M. J; HECKENLIVELY, J. R et al.Cytogenetics and cell genetics. 1999, Vol 84, Num 1-2, pp 22-27, issn 0301-0171Article

Analysis of the OA1 gene reveals mutations in only one-third of patients with X-linked ocular albinismSCHIAFFINO, M. V; BASSI, M. T; LEWIS, R. A et al.Human molecular genetics (Print). 1995, Vol 4, Num 12, pp 2319-2325, issn 0964-6906Article

Maximum-likelihood estimation in linkage heterogeneity models including additional information via the EM algorithmHOUWING-DUISTERMAAT, J. J; SANDKUIJL, L. A; BERGEN, A. A. B et al.Genetic epidemiology. 1995, Vol 12, Num 5, pp 515-527, issn 0741-0395Article

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

Additional evidence for a gene locus for progressive cone dystrophy with late rod involvement in Xp21.1-p11.3BERGEN, A. A. B; MEIRE, F; TEN BRINK, J et al.Genomics (San Diego, Calif.). 1993, Vol 18, Num 2, pp 463-464, issn 0888-7543Article

Refinement of the localization of the X-linked ocular albinism geneBERGEN, A. A. B; ZIJP, P; SCHUURMAN, E. J. M et al.Genomics (San Diego, Calif.). 1993, Vol 16, Num 1, pp 272-273, issn 0888-7543Article

Multipoint linkage analysis in X-linked ocular albinism of the Nettleship-Falls typeBERGEN, A. A. B; SAMANNS, C; SCHUURMAN, E. J. M et al.Human genetics. 1991, Vol 88, Num 2, pp 162-166, issn 0340-6717Article

Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)HOLLANDER, A. I. D; TEN BRINK, J. B; HOYNG, C. B et al.Nature genetics. 1999, Vol 23, Num 2, pp 217-221, issn 1061-4036Article

Exclusion of PPEF as the gene causing X-linked juvenile retinoschisisVAN DE VOSSE, E; FRANCO, B; BERGEN, A. A. B et al.Human genetics. 1997, Vol 101, Num 2, pp 235-237, issn 0340-6717Article

Correlation of phenotype with genotype in inherited retinal degenerationDAIGER, S. P; SULLIVAN, L. S; RODRIGUEZ, J. A et al.Behavioral and brain sciences (Print). 1995, Vol 18, Num 3, pp 452-467, issn 0140-525XArticle

Nance-Horan syndrome : linkage analysis in family from the NetherlandsBERGEN, A. A. B; TEN BRINK, J; SCHUURMAN, E. J. M et al.Genomics (San Diego, Calif.). 1994, Vol 21, Num 1, pp 238-240, issn 0888-7543Article

X linked progressive cone dystrophy : localisation of the gene locus to Xp21-p11.1 by linkage analysisMEIRE, F. M; BERGEN, A. A. B; DE ROUCK, A et al.British journal of ophthalmology. 1994, Vol 78, Num 2, pp 103-108, issn 0007-1161Article