Bleeker-Wagemakers EM - Search Results

1

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

2

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

3

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

4

Localization of the X-linked ocular albinism gene (OA1) between DXS278/DXS237 and DXS143/DXS16 by linkage analysis.

Bergen AA, Samanns C, Van Dorp DB, Ferguson-Smith MA, Gal A, Bleeker-Wagemakers EM. Bergen AA, et al. Ophthalmic Paediatr Genet. 1990 Sep;11(3):165-70. doi: 10.3109/13816819009020975. Ophthalmic Paediatr Genet. 1990. PMID: 2280973

5

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

6

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. Cytogenet Cell Genet. 1996;73(1-2):81-5. doi: 10.1159/000134313. Cytogenet Cell Genet. 1996. PMID: 8646891

7

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: bleeker wagemakers em. Cytogenet Cell Genet. 1999;84(1-2):22-7. doi: 10.1159/000015204. Cytogenet Cell Genet. 1999. PMID: 10343093

8

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. Ophthalmic Paediatr Genet. 1992 Dec;13(4):227-36. doi: 10.3109/13816819209105171. Ophthalmic Paediatr Genet. 1992. PMID: 1488223

9

Multipoint linkage analysis in X-linked ocular albinism of the Nettleship-Falls type.

Bergen AA, Samanns C, Schuurman EJ, van Osch L, van Dorp DB, Pinckers AJ, Bakker E, Gal A, van Ommen GJ, Bleeker-Wagemakers EM. Bergen AA, et al. Hum Genet. 1991 Dec;88(2):162-6. doi: 10.1007/BF00206065. Hum Genet. 1991. PMID: 1684563

10

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

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