Schuurman EJ - Search Results

1

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. Among authors: schuurman ej. Hum Genet. 1991 Dec;88(2):162-6. doi: 10.1007/BF00206065. Hum Genet. 1991. PMID: 1684563

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. Among authors: schuurman ej. Clin Genet. 1992 Mar;41(3):135-8. doi: 10.1111/j.1399-0004.1992.tb03649.x. Clin Genet. 1992. PMID: 1348665

3

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. Among authors: schuurman ej. Ophthalmic Genet. 1995 Jun;16(2):63-70. doi: 10.3109/13816819509056914. Ophthalmic Genet. 1995. PMID: 7493158

4

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

5

DNA carrier detection in X-linked progressive cone dystrophy.

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

6

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. Among authors: schuurman ej. Cytogenet Cell Genet. 1993;62(4):231-5. doi: 10.1159/000133484. Cytogenet Cell Genet. 1993. PMID: 8440142

7

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. Among authors: schuurman ej. Genomics. 1993 Apr;16(1):272-3. doi: 10.1006/geno.1993.1176. Genomics. 1993. PMID: 8486373

8

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. Among authors: schuurman ej. Genomics. 1994 May 1;21(1):238-40. doi: 10.1006/geno.1994.1248. Genomics. 1994. PMID: 8088793

9

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. Among authors: schuurman ej. Genomics. 1993 Nov;18(2):463-4. doi: 10.1006/geno.1993.1504. Genomics. 1993. PMID: 8288262 No abstract available.

10

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. Among authors: schuurman ej. 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.

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