Bergen AA - Search Results

1

Characterization of SCML1, a new gene in Xp22, with homology to developmental polycomb genes.

van de Vosse E, Walpole SM, Nicolaou A, van der Bent P, Cahn A, Vaudin M, Ross MT, Durham J, Pavitt R, Wilkinson J, Grafham D, Bergen AA, van Ommen GJ, Yates JR, den Dunnen JT, Trump D. van de Vosse E, et al. Among authors: bergen aa. Genomics. 1998 Apr 1;49(1):96-102. doi: 10.1006/geno.1998.5224. Genomics. 1998. PMID: 9570953

2

Exclusion of PPEF as the gene causing X-linked juvenile retinoschisis.

van de Vosse E, Franco B, van der Bent P, Montini E, Orth U, Hanauer A, Tijmes N, van Ommen GJ, Ballabio A, den Dunnen JT, Bergen AA. van de Vosse E, et al. Among authors: bergen aa. Hum Genet. 1997 Dec;101(2):235-7. doi: 10.1007/s004390050622. Hum Genet. 1997. PMID: 9402977

3

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.

4

Refinement of the localization of the X-linked ocular albinism gene.

Bergen AA, Zijp P, Schuurman EJ, Bleeker-Wagemakers EM, Apkarian P, van Ommen GJ. Bergen AA, et al. Genomics. 1993 Apr;16(1):272-3. doi: 10.1006/geno.1993.1176. Genomics. 1993. PMID: 8486373

5

An Xp22.1-p22.2 YAC contig encompassing the disease loci for RS, KFSD, CLS, HYP and RP15: refined localization of RS.

Van de Vosse E, Bergen AA, Meershoek EJ, Oosterwijk JC, Gregory S, Bakker B, Weissenbach J, Coffey AJ, van Ommen GJ, Den Dunnen JT. Van de Vosse E, et al. Among authors: bergen aa. Eur J Hum Genet. 1996;4(2):101-4. doi: 10.1159/000472177. Eur J Hum Genet. 1996. PMID: 8744027

6

Analysis of the OA1 gene reveals mutations in only one-third of patients with X-linked ocular albinism.

Schiaffino MV, Bassi MT, Galli L, Renieri A, Bruttini M, De Nigris F, Bergen AA, Charles SJ, Yates JR, Meindl A, et al. Schiaffino MV, et al. Among authors: bergen aa. Hum Mol Genet. 1995 Dec;4(12):2319-25. doi: 10.1093/hmg/4.12.2319. Hum Mol Genet. 1995. PMID: 8634705

7

Carrier detection in X-linked retinitis pigmentosa by multipoint DNA analysis. Problems due to genetic heterogeneity.

Bergen AA, Platje EJ, Craig I, Bakker E, Bleeker-Wagemakers EM, van Ommen GJ. Bergen AA, et al. Ophthalmic Paediatr Genet. 1991 Jun;12(2):99-103. doi: 10.3109/13816819109023681. Ophthalmic Paediatr Genet. 1991. PMID: 1923320

8

A submicroscopic deletion in a patient with isolated X-linked ocular albinism (OA1).

Bassi MT, Bergen AA, Wapenaar MC, Schiaffino MV, van Schooneveld M, Yates JR, Charles SJ, Meitinger T, Ballabio A. Bassi MT, et al. Among authors: bergen aa. Hum Mol Genet. 1994 Apr;3(4):647-8. doi: 10.1093/hmg/3.4.647. Hum Mol Genet. 1994. PMID: 8069311 No abstract available.

9

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

10

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

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