Wieringa B - Search Results

1

Genetic and physical mapping of a novel region close to the fragile X site on the human X chromosome.

Patterson MN, Bell MV, Bloomfield J, Flint T, Dorkins H, Thibodeau SN, Schaid D, Bren G, Schwartz CE, Wieringa B, et al. Patterson MN, et al. Among authors: wieringa b. Genomics. 1989 May;4(4):570-8. doi: 10.1016/0888-7543(89)90281-4. Genomics. 1989. PMID: 2744766

2

New polymorphic DNA marker close to the fragile site FRAXA.

Oostra BA, Hupkes PE, Perdon LF, van Bennekom CA, Bakker E, Halley DJ, Schmidt M, Du Sart D, Smits A, Wieringa B, et al. Oostra BA, et al. Among authors: wieringa b. Genomics. 1990 Jan;6(1):129-32. doi: 10.1016/0888-7543(90)90457-6. Genomics. 1990. PMID: 1968042 Free article.

3

Physical and genetic mapping of a novel chromosome 19 ERCC1 marker showing close linkage with myotonic dystrophy.

Shutler G, MacKenzie AE, Brunner H, Wieringa B, de Jong P, Lohman FP, Leblond S, Bailly J, Korneluk RG. Shutler G, et al. Among authors: wieringa b. Genomics. 1991 Mar;9(3):500-4. doi: 10.1016/0888-7543(91)90416-c. Genomics. 1991. PMID: 1674498

4

Evidence for linkage of the central core disease locus to the proximal long arm of human chromosome 19.

Kausch K, Lehmann-Horn F, Janka M, Wieringa B, Grimm T, Müller CR. Kausch K, et al. Among authors: wieringa b. Genomics. 1991 Jul;10(3):765-9. doi: 10.1016/0888-7543(91)90461-m. Genomics. 1991. PMID: 1889818

5

High-resolution physical mapping of four microsatellite repeat markers near the RYR1 locus on chromosome 19q13.1 and apparent exclusion of the MHS locus from this region in two malignant hyperthermia susceptible families.

Iles DE, Segers B, Heytens L, Sengers RC, Wieringa B. Iles DE, et al. Among authors: wieringa b. Genomics. 1992 Nov;14(3):749-54. doi: 10.1016/s0888-7543(05)80179-x. Genomics. 1992. PMID: 1427902

6

Physical mapping and cloning of the proximal segment of the myotonic dystrophy gene region.

Shutler G, Korneluk RG, Tsilfidis C, Mahadevan M, Bailly J, Smeets H, Jansen G, Wieringa B, Lohman F, Aslanidis C, et al. Shutler G, et al. Among authors: wieringa b. Genomics. 1992 Jul;13(3):518-25. doi: 10.1016/0888-7543(92)90119-d. Genomics. 1992. PMID: 1639380

7

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

8

A multipoint linkage map around the locus for myotonic dystrophy on chromosome 19.

Brunner HG, Smeets H, Lambermon HM, Coerwinkel-Driessen M, van Oost BA, Wieringa B, Ropers HH. Brunner HG, et al. Among authors: wieringa b. Genomics. 1989 Oct;5(3):589-95. doi: 10.1016/0888-7543(89)90027-x. Genomics. 1989. PMID: 2575588

9

The ubiquitous mitochondrial creatine kinase gene maps to a conserved region on human chromosome 15q15 and mouse chromosome 2 bands F1-F3.

Steeghs K, Merkx G, Wieringa B. Steeghs K, et al. Among authors: wieringa b. Genomics. 1994 Nov 1;24(1):193-5. doi: 10.1006/geno.1994.1604. Genomics. 1994. PMID: 7896282 No abstract available.

10

Refined localization of the alpha 1-subunit of the skeletal muscle L-type voltage-dependent calcium channel (CACNL1A3) to human chromosome 1q32 by in situ hybridization.

Iles DE, Segers B, Olde Weghuis D, Suijkerbuijk R, Mikala G, Schwartz A, Wieringa B. Iles DE, et al. Among authors: wieringa b. Genomics. 1994 Feb;19(3):561-3. doi: 10.1006/geno.1994.1106. Genomics. 1994. PMID: 8188298

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