Wieringa B - Search Results

1

Molecular analysis of male-viable deletions and duplications allows ordering of 52 DNA probes on proximal Xq.

Cremers FP, van de Pol TJ, Wieringa B, Hofker MH, Pearson PL, Pfeiffer RA, Mikkelsen M, Tabor A, Ropers HH. Cremers FP, et al. Among authors: wieringa b. Am J Hum Genet. 1988 Oct;43(4):452-61. Am J Hum Genet. 1988. PMID: 3177387 Free PMC article.

2

Cloning of the breakpoints of a deletion associated with choroidermia.

Cremers FP, Brunsmann F, Berger W, van Kerkhoff EP, van de Pol TJ, Wieringa B, Pawlowitzki IH, Ropers HH. Cremers FP, et al. Among authors: wieringa b. Hum Genet. 1990 Nov;86(1):61-4. doi: 10.1007/BF00205174. Hum Genet. 1990. PMID: 1979308

3

Cloning of a gene that is rearranged in patients with choroideraemia.

Cremers FP, van de Pol DJ, van Kerkhoff LP, Wieringa B, Ropers HH. Cremers FP, et al. Among authors: wieringa b. Nature. 1990 Oct 18;347(6294):674-7. doi: 10.1038/347674a0. Nature. 1990. PMID: 2215697

4

Deletions in patients with classical choroideremia vary in size from 45 kb to several megabases.

Cremers FP, Sankila EM, Brunsmann F, Jay M, Jay B, Wright A, Pinckers AJ, Schwartz M, van de Pol DJ, Wieringa B, et al. Cremers FP, et al. Among authors: wieringa b. Am J Hum Genet. 1990 Oct;47(4):622-8. Am J Hum Genet. 1990. PMID: 2220804 Free PMC article.

5

Use of variable simple sequence motifs as genetic markers: application to study of myotonic dystrophy.

Smeets HJ, Brunner HG, Ropers HH, Wieringa B. Smeets HJ, et al. Among authors: wieringa b. Hum Genet. 1989 Oct;83(3):245-51. doi: 10.1007/BF00285165. Hum Genet. 1989. PMID: 2571562

6

Physical fine-mapping of a deletion spanning the Norrie gene.

Diergaarde PJ, Wieringa B, Bleeker-Wagemakers EM, Sims KB, Breakefield XO, Ropers HH. Diergaarde PJ, et al. Among authors: wieringa b. Hum Genet. 1989 Dec;84(1):22-6. doi: 10.1007/BF00210665. Hum Genet. 1989. PMID: 2606473

7

The gene for X-linked progressive mixed deafness with perilymphatic gusher during stapes surgery (DFN3) is linked to PGK.

Brunner HG, van Bennekom A, Lambermon EM, Oei TL, Cremers WR, Wieringa B, Ropers HH. Brunner HG, et al. Among authors: wieringa b. Hum Genet. 1988 Dec;80(4):337-40. doi: 10.1007/BF00273647. Hum Genet. 1988. PMID: 2904400

8

Physical fine mapping of the choroideremia locus using Xq21 deletions associated with complex syndromes.

Cremers FP, van de Pol DJ, Diergaarde PJ, Wieringa B, Nussbaum RL, Schwartz M, Ropers HH. Cremers FP, et al. Among authors: wieringa b. Genomics. 1989 Jan;4(1):41-6. doi: 10.1016/0888-7543(89)90312-1. Genomics. 1989. PMID: 2914708

9

Tight linkage between myotonic dystrophy and apolipoprotein E genes revealed with allele-specific oligonucleotides.

Smeets B, Poddighe J, Brunner H, Ropers HH, Wieringa B. Smeets B, et al. Among authors: wieringa b. Hum Genet. 1988 Sep;80(1):49-52. doi: 10.1007/BF00451455. Hum Genet. 1988. PMID: 3417303

10

An interstitial duplication of the X chromosome in a male allows physical fine mapping of probes from the Xq13-q22 region.

Cremers FP, Pfeiffer RA, van de Pol TJ, Hofker MH, Kruse TA, Wieringa B, Ropers HH. Cremers FP, et al. Among authors: wieringa b. Hum Genet. 1987 Sep;77(1):23-7. doi: 10.1007/BF00284707. Hum Genet. 1987. PMID: 3476455

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