Bergen AA - Search Results

1

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 pseudogenes.

van Soest S, van Rossem MJ, Heckenlively JR, van den Born LI, de Meulemeester TM, Vliex S, de Jong PT, Bleeker-Wagemakers EM, Westerveld A, Bergen AA. van Soest S, et al. Among authors: bergen aa. Cytogenet Cell Genet. 1999;84(1-2):22-7. doi: 10.1159/000015204. Cytogenet Cell Genet. 1999. PMID: 10343093

2

Detection of a new submicroscopic Norrie disease deletion interval with a novel DNA probe isolated by differential Alu PCR fingerprint cloning.

Bergen AA, Wapenaar MC, Schuurman EJ, Diergaarde PJ, Lerach H, Monaco AP, Bakker E, Bleeker-Wagemakers EM, van Ommen GJ. Bergen AA, et al. Cytogenet Cell Genet. 1993;62(4):231-5. doi: 10.1159/000133484. Cytogenet Cell Genet. 1993. PMID: 8440142

3

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 LI, Bleeker-Wagemakers EM, Sharp E, Sandkuijl LA, Westerveld A, Bergen AA. van Soest S, et al. Among authors: bergen aa. Cytogenet Cell Genet. 1996;73(1-2):81-5. doi: 10.1159/000134313. Cytogenet Cell Genet. 1996. PMID: 8646891

4

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: bergen aa. Nat Genet. 1999 Oct;23(2):217-21. doi: 10.1038/13848. Nat Genet. 1999. PMID: 10508521

5

A retrospective study of registered retinitis pigmentosa patients in The Netherlands.

van den Born LI, Bergen AA, Bleeker-Wagemakers EM. van den Born LI, et al. Among authors: bergen aa. Ophthalmic Paediatr Genet. 1992 Dec;13(4):227-36. doi: 10.3109/13816819209105171. Ophthalmic Paediatr Genet. 1992. PMID: 1488223

6

Assignment of a gene for autosomal recessive retinitis pigmentosa (RP12) to chromosome 1q31-q32.1 in an inbred and genetically heterogeneous disease population.

van Soest S, van den Born LI, Gal A, Farrar GJ, Bleeker-Wagemakers LM, Westerveld A, Humphries P, Sandkuijl LA, Bergen AA. van Soest S, et al. Among authors: bergen aa. Genomics. 1994 Aug;22(3):499-504. doi: 10.1006/geno.1994.1422. Genomics. 1994. PMID: 8001962

7

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

8

Multipoint linkage analysis in X-linked juvenile retinoschisis.

Bergen AA, van Schooneveld MJ, Orth U, Bleeker-Wagemakers EM, Gal A. Bergen AA, et al. Clin Genet. 1993 Mar;43(3):113-6. doi: 10.1111/j.1399-0004.1993.tb04433.x. Clin Genet. 1993. PMID: 8500256

9

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. 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.

10

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: bergen aa. Am J Hum Genet. 1997 Oct;61(4):934-9. doi: 10.1086/514884. Am J Hum Genet. 1997. PMID: 9382106 Free PMC article.

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