Wapenaar MC - Search Results

1

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

2

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.

3

The X chromosome shows less genetic variation at restriction sites than the autosomes.

Hofker MH, Skraastad MI, Bergen AA, Wapenaar MC, Bakker E, Millington-Ward A, van Ommen GJ, Pearson PL. Hofker MH, et al. Among authors: wapenaar mc. Am J Hum Genet. 1986 Oct;39(4):438-51. Am J Hum Genet. 1986. PMID: 2876629 Free PMC article.

4

AK1 detects a VNTR locus in the pseudoautosomal region.

Klink A, Wapenaar M, van Ommen GJ, Rappold G. Klink A, et al. Hum Mol Genet. 1993 Mar;2(3):339. doi: 10.1093/hmg/2.3.339-a. Hum Mol Genet. 1993. PMID: 8098983 No abstract available.

5

Isolation and characterization of cell hybrids containing human Xp-chromosome fragments.

Wapenaar MC, Kievits T, Meera Khan P, Pearson PL, Van Ommen GJ. Wapenaar MC, et al. Cytogenet Cell Genet. 1990;54(1-2):10-4. doi: 10.1159/000132945. Cytogenet Cell Genet. 1990. PMID: 2249469

6

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

7

Deletions within the pseudoautosomal region help map three new markers and indicate a possible role of this region in linear growth.

Henke A, Wapenaar M, van Ommen GJ, Maraschio P, Camerino G, Rappold G. Henke A, et al. Am J Hum Genet. 1991 Oct;49(4):811-9. Am J Hum Genet. 1991. PMID: 1897527 Free PMC article.

8

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.

9

A CA-repeat polymorphism near DXS418 (P122).

Van De Vosse E, Booms PF, Vossen RH, Wapenaar MC, Van Ommen GJ, Den Dunnen JT. Van De Vosse E, et al. Among authors: wapenaar mc. Hum Mol Genet. 1993 Dec;2(12):2202. doi: 10.1093/hmg/2.12.2202-a. Hum Mol Genet. 1993. PMID: 8111402 No abstract available.

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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