Ten Brink JB - Search Results

1

Molecular Inversion Probe-Based Sequencing of USH2A Exons and Splice Sites as a Cost-Effective Screening Tool in USH2 and arRP Cases.

Reurink J, Dockery A, Oziębło D, Farrar GJ, Ołdak M, Ten Brink JB, Bergen AA, Rinne T, Yntema HG, Pennings RJE, van den Born LI, Aben M, Oostrik J, Venselaar H, Plomp AS, Khan MI, van Wijk E, Cremers FPM, Roosing S, Kremer H. Reurink J, et al. Among authors: ten brink jb. Int J Mol Sci. 2021 Jun 15;22(12):6419. doi: 10.3390/ijms22126419. Int J Mol Sci. 2021. PMID: 34203967 Free PMC article.

2

Localization of a novel X-linked congenital stationary night blindness locus: close linkage to the RP3 type retinitis pigmentosa gene region.

Bergen AA, ten Brink JB, Riemslag F, Schuurman EJ, Tijmes N. Bergen AA, et al. Among authors: ten brink jb. Hum Mol Genet. 1995 May;4(5):931-5. doi: 10.1093/hmg/4.5.931. Hum Mol Genet. 1995. PMID: 7633454

3

Efficient DNA carrier detection in X linked juvenile retinoschisis.

Bergen AA, ten Brink JB, van Schooneveld MJ. Bergen AA, et al. Among authors: ten brink jb. Br J Ophthalmol. 1995 Jul;79(7):683-6. doi: 10.1136/bjo.79.7.683. Br J Ophthalmol. 1995. PMID: 7662636 Free PMC article.

4

Refinement of the chromosomal position of the X linked juvenile retinoschisis gene.

Bergen AA, ten Brink JB, Bleeker-Wagemakers LM, van Schooneveld MJ. Bergen AA, et al. Among authors: ten brink jb. J Med Genet. 1994 Dec;31(12):972-5. doi: 10.1136/jmg.31.12.972. J Med Genet. 1994. PMID: 7891384 Free PMC article.

5

Nance-Horan syndrome: linkage analysis in a family from The Netherlands.

Bergen AA, ten Brink J, Schuurman EJ, Bleeker-Wagemakers EM. Bergen AA, et al. Genomics. 1994 May 1;21(1):238-40. doi: 10.1006/geno.1994.1248. Genomics. 1994. PMID: 8088793

6

Additional evidence for a gene locus for progressive cone dystrophy with late rod involvement in Xp21.1-p11.3.

Bergen AA, Meire F, ten Brink J, Schuurman EJ, van Ommen GJ, Delleman JW. Bergen AA, et al. Genomics. 1993 Nov;18(2):463-4. doi: 10.1006/geno.1993.1504. Genomics. 1993. PMID: 8288262 No abstract available.

7

Conclusive evidence for a distinct congenital stationary night blindness locus in Xp21.1.

Bergen AA, ten Brink JB, Riemslag F, Schuurman EJ, Meire F, Tijmes N, de Jong PT. Bergen AA, et al. Among authors: ten brink jb. J Med Genet. 1996 Oct;33(10):869-72. doi: 10.1136/jmg.33.10.869. J Med Genet. 1996. PMID: 8933343 Free PMC article.

8

A gene for X-linked optic atrophy is closely linked to the Xp11.4-Xp11.2 region of the X chromosome.

Assink JJ, Tijmes NT, ten Brink JB, Oostra RJ, Riemslag FC, de Jong PT, Bergen AA. Assink JJ, et al. Among authors: ten brink jb. Am J Hum Genet. 1997 Oct;61(4):934-9. doi: 10.1086/514884. Am J Hum Genet. 1997. PMID: 9382106 Free PMC article.

9

Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12).

den Hollander AI, ten Brink JB, de Kok YJ, van Soest S, van den Born LI, van Driel MA, van de Pol DJ, Payne AM, Bhattacharya SS, Kellner U, Hoyng CB, Westerveld A, Brunner HG, Bleeker-Wagemakers EM, Deutman AF, Heckenlively JR, Cremers FP, Bergen AA. den Hollander AI, et al. Among authors: ten brink jb. Nat Genet. 1999 Oct;23(2):217-21. doi: 10.1038/13848. Nat Genet. 1999. PMID: 10508521

10

Mutations in ABCC6 cause pseudoxanthoma elasticum.

Bergen AA, Plomp AS, Schuurman EJ, Terry S, Breuning M, Dauwerse H, Swart J, Kool M, van Soest S, Baas F, ten Brink JB, de Jong PT. Bergen AA, et al. Among authors: ten brink jb. Nat Genet. 2000 Jun;25(2):228-31. doi: 10.1038/76109. Nat Genet. 2000. PMID: 10835643

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