Bergen AA - Search Results

1

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.

2

Identification of mutations in the AIPL1, CRB1, GUCY2D, RPE65, and RPGRIP1 genes in patients with juvenile retinitis pigmentosa.

Booij JC, Florijn RJ, ten Brink JB, Loves W, Meire F, van Schooneveld MJ, de Jong PT, Bergen AA. Booij JC, et al. Among authors: bergen aa. J Med Genet. 2005 Nov;42(11):e67. doi: 10.1136/jmg.2005.035121. J Med Genet. 2005. PMID: 16272259 Free PMC article.

3

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.

4

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

5

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.

6

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.

7

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

8

Multipoint linkage analysis and homogeneity tests in 15 Dutch X-linked retinitis pigmentosa families.

Bergen AA, Van den Born LI, Schuurman EJ, Pinckers AJ, Van Ommen GJ, Bleekers-Wagemakers EM, Sandkuijl LA. Bergen AA, et al. Ophthalmic Genet. 1995 Jun;16(2):63-70. doi: 10.3109/13816819509056914. Ophthalmic Genet. 1995. PMID: 7493158

9

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. Hum Mol Genet. 1995 May;4(5):931-5. doi: 10.1093/hmg/4.5.931. Hum Mol Genet. 1995. PMID: 7633454

10

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.

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