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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

Retinitis pigmentosa : Defined from a molecular point of viewVAN SOEST, S; WESTERVELD, A; DE JONG, P. T. V. M et al.Survey of ophthalmology. 1999, Vol 43, Num 4, pp 321-334, issn 0039-6257Article

Positional cloning of the gene for X-linked retinitis pigmentosa 2SCHWAHN, U; LENZNER, S; PINCKERS, A. J. L. G et al.Nature genetics. 1998, Vol 19, Num 4, pp 327-332, issn 1061-4036Article

A gene for X-linked optic atrophy is closely linked to the Xp11.4-Xp11.2 region of the X chromosomeASSINK, J. J. M; TIJMES, N. T; TEN BRINK, J. B et al.American journal of human genetics. 1997, Vol 61, Num 4, pp 934-939, issn 0002-9297Article

Fine mapping of the autosomal recessive retinitis pigmentosa locus (RP12) on chromosome 1q ; exclusion of the phosducin gene (PDC)VAN SOEST, S; TE NIJENHUIS, S; VAN DEN BORN, L. I et al.Cytogenetics and cell genetics. 1996, Vol 73, Num 1-2, pp 81-85, issn 0301-0171Article

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

Future directions for rhodopsin structure and function studiesHARGRAVE, P. A.Behavioral and brain sciences (Print). 1995, Vol 18, Num 3, pp 403-414, issn 0140-525XArticle

Do the calmodulin-stimulated adenylyl cyclases play a role in neuroplasticity ?XIA, Z; CHOI, E.-J; STORM, D. R et al.Behavioral and brain sciences (Print). 1995, Vol 18, Num 3, pp 429-440, issn 0140-525XArticle

Carrier detection in X-linked ocular albinism of the nettleship-falls type by DNA analysisBERGEN, A. A. B; SCHUURMAN, E. J. M; VAN DEN BORN, L. I et al.Clinical genetics. 1992, Vol 41, Num 3, pp 135-138, issn 0009-9163Article

Efficient isolation of X chromosome-specific single-copy probes from a cosmid library of a human X/hamster hybrid cell line: mapping of new probles close to the locus for X-linked mental retardationHOFKER, M. H; BERGEN, A. A. B; SKRAASTAD, M. I et al.American journal of human genetics. 1987, Vol 40, Num 4, pp 312-328, issn 0002-9297Article

Sorsby fundus dystrophy without a mutation in the TIMP-3 geneASSINK, J. J. M; DE BACKER, E; TEN BRINK, J. B et al.British journal of ophthalmology. 2000, Vol 84, Num 7, pp 682-686, issn 0007-1161Article

The 2588G→C mutation in the ABCR gene is a mild frequent founder mutation in the western European population and allows the classification of ABCR mutations in patients with Stargardt diseaseMAUGERI, A; VAN DRIEL, M. A; DAHL, N et al.American journal of human genetics. 1999, Vol 64, Num 4, pp 1024-1035, issn 0002-9297Article

The mutation spectrum of the bestrophin protein : functional implicationsBAKALL, B; MARKNELL, T; WADELIUS, C et al.Human genetics. 1999, Vol 104, Num 5, pp 383-389, issn 0340-6717Article