Bergen AA - Search Results

1

Proposal for updating the pseudoxanthoma elasticum classification system and a review of the clinical findings.

Plomp AS, Toonstra J, Bergen AA, van Dijk MR, de Jong PT. Plomp AS, et al. Among authors: bergen aa. Am J Med Genet A. 2010 Apr;152A(4):1049-58. doi: 10.1002/ajmg.a.33329. Am J Med Genet A. 2010. PMID: 20358627 Review.

2

Carrier detection in X-linked ocular albinism of the Nettleship-Falls type by DNA analysis.

Bergen AA, Schuurman EJ, van den Born LI, Samanns C, van Dorp DB, Pinckers AJ, Bakker E, van Ommen GJ, Gal A, Bleeker-Wagemakers EM. Bergen AA, et al. Clin Genet. 1992 Mar;41(3):135-8. doi: 10.1111/j.1399-0004.1992.tb03649.x. Clin Genet. 1992. PMID: 1348665

3

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

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. 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

Identification of a key recombinant which assigns the incomplete congenital stationary night blindness gene proximal to MAOB.

Bergen AA, Kestelyn P, Leys M, Meire F. Bergen AA, et al. J Med Genet. 1994 Jul;31(7):580-2. doi: 10.1136/jmg.31.7.580. J Med Genet. 1994. PMID: 7966198 Free PMC article.

6

DNA carrier detection in X-linked progressive cone dystrophy.

Bergen AA, Meire F, Schuurman EJ, Delleman JW. Bergen AA, et al. Clin Genet. 1994 May;45(5):236-40. doi: 10.1111/j.1399-0004.1994.tb04148.x. Clin Genet. 1994. PMID: 8076408

7

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

8

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.

9

A locus for autosomal recessive pseudoxanthoma elasticum, with penetrance of vascular symptoms in carriers, maps to chromosome 16p13.1.

van Soest S, Swart J, Tijmes N, Sandkuijl LA, Rommers J, Bergen AA. van Soest S, et al. Among authors: bergen aa. Genome Res. 1997 Aug;7(8):830-4. doi: 10.1101/gr.7.8.830. Genome Res. 1997. PMID: 9267806 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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