Wapenaar MC - Search Results

1

Deletion screening in patients with Duchenne muscular dystrophy.

Wulff K, Herrmann FH, Wapenaar MC, Wehnert M. Wulff K, et al. Among authors: wapenaar mc. J Neurol. 1989 Dec;236(8):470-3. doi: 10.1007/BF00328509. J Neurol. 1989. PMID: 2614492

2

Duchenne muscular dystrophy: high frequency of deletions.

Bartlett RJ, Pericak-Vance MA, Koh J, Yamaoka LH, Chen JC, Hung WY, Speer MC, Wapenaar MC, Van Ommen GJ, Bakker E, et al. Bartlett RJ, et al. Among authors: wapenaar mc. Neurology. 1988 Jan;38(1):1-4. doi: 10.1212/wnl.38.1.1. Neurology. 1988. PMID: 3275902

3

Molecular deletions in the Duchenne/Becker muscular dystrophy gene.

Hart KA, Abbs S, Wapenaar MC, Cole CG, Hodgson SV, Bobrow M. Hart KA, et al. Among authors: wapenaar mc. Clin Genet. 1989 Apr;35(4):251-60. doi: 10.1111/j.1399-0004.1989.tb02939.x. Clin Genet. 1989. PMID: 2653672 Review.

4

A deletion hot spot in the Duchenne muscular dystrophy gene.

Wapenaar MC, Kievits T, Hart KA, Abbs S, Blonden LA, den Dunnen JT, Grootscholten PM, Bakker E, Verellen-Dumoulin C, Bobrow M, et al. Wapenaar MC, et al. Genomics. 1988 Feb;2(2):101-8. doi: 10.1016/0888-7543(88)90090-0. Genomics. 1988. PMID: 2900805

5

Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications.

Den Dunnen JT, Grootscholten PM, Bakker E, Blonden LA, Ginjaar HB, Wapenaar MC, van Paassen HM, van Broeckhoven C, Pearson PL, van Ommen GJ. Den Dunnen JT, et al. Among authors: wapenaar mc. Am J Hum Genet. 1989 Dec;45(6):835-47. Am J Hum Genet. 1989. PMID: 2573997 Free PMC article.

6

Molecular-genetic study of Duchenne and Becker muscular dystrophies: deletion analyses of 45 Japanese patients and segregation analyses in their families with RFLPs based on the data from normal Japanese females.

Sugino S, Fujishita S, Kamimura N, Matsumoto T, Wapenaar MC, Deng HX, Shibuya N, Miike T, Niikawa N. Sugino S, et al. Among authors: wapenaar mc. Am J Med Genet. 1989 Dec;34(4):555-61. doi: 10.1002/ajmg.1320340421. Am J Med Genet. 1989. PMID: 2576185

7

High resolution deletion breakpoint mapping in the DMD gene by whole cosmid hybridization.

Blonden LA, den Dunnen JT, van Paassen HM, Wapenaar MC, Grootscholten PM, Ginjaar HB, Bakker E, Pearson PL, van Ommen GJ. Blonden LA, et al. Among authors: wapenaar mc. Nucleic Acids Res. 1989 Jul 25;17(14):5611-21. doi: 10.1093/nar/17.14.5611. Nucleic Acids Res. 1989. PMID: 2569720 Free PMC article.

8

Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy.

Hofker MH, Wapenaar MC, Goor N, Bakker E, van Ommen GJ, Pearson PL. Hofker MH, et al. Among authors: wapenaar mc. Hum Genet. 1985;70(2):148-56. doi: 10.1007/BF00273073. Hum Genet. 1985. PMID: 2989153

9

Physical mapping of 14 new DNA markers isolated from the human distal Xp region.

Wapenaar MC, Petit C, Basler E, Ballabio A, Henke A, Rappold GA, van Paassen HM, Blonden LA, van Ommen GJ. Wapenaar MC, et al. Genomics. 1992 May;13(1):167-75. doi: 10.1016/0888-7543(92)90217-g. Genomics. 1992. PMID: 1349572

10

A high resolution deletion map of human chromosome Xp22.

Schaefer L, Ferrero GB, Grillo A, Bassi MT, Roth EJ, Wapenaar MC, van Ommen GJ, Mohandas TK, Rocchi M, Zoghbi HY, Ballabio A. Schaefer L, et al. Among authors: wapenaar mc. Nat Genet. 1993 Jul;4(3):272-9. doi: 10.1038/ng0793-272. Nat Genet. 1993. PMID: 8358436

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