Bakker E - Search Results

1

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: bakker e. Neurology. 1988 Jan;38(1):1-4. doi: 10.1212/wnl.38.1.1. Neurology. 1988. PMID: 3275902

2

An unusual variant of Becker muscular dystrophy.

de Visser M, Bakker E, Defesche JC, Bolhuis PA, van Ommen GJ. de Visser M, et al. Among authors: bakker e. Ann Neurol. 1990 May;27(5):578-81. doi: 10.1002/ana.410270521. Ann Neurol. 1990. PMID: 2193611

3

Prenatal diagnosis of Duchenne muscular dystrophy: a three-year experience in a rapidly evolving field.

Bakker E, Bonten EJ, Veenema H, den Dunnen JT, Grootscholten PM, van Ommen GJ, Pearson PL. Bakker E, et al. J Inherit Metab Dis. 1989;12 Suppl 1:174-90. doi: 10.1007/BF01799293. J Inherit Metab Dis. 1989. PMID: 2509804 Review.

4

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: bakker e. Am J Hum Genet. 1989 Dec;45(6):835-47. Am J Hum Genet. 1989. PMID: 2573997 Free PMC article.

5

Development of additional RFLP probes near the locus for Duchenne muscular dystrophy by cosmid cloning of the DXS84 (754) locus.

Hofker MH, van Ommen GJ, Bakker E, Burmeister M, Pearson PL. Hofker MH, et al. Among authors: bakker e. Hum Genet. 1986 Nov;74(3):270-4. doi: 10.1007/BF00282547. Hum Genet. 1986. PMID: 2877935

6

DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure.

Bakker E, Bonten EJ, De Lange LF, Veenema H, Majoor-Krakauer D, Hofker MH, Van Ommen GJ, Pearson PL. Bakker E, et al. J Med Genet. 1986 Dec;23(6):573-80. doi: 10.1136/jmg.23.6.573. J Med Genet. 1986. PMID: 2879929 Free PMC article.

7

Carrier detection and gene analysis of Duchenne muscular dystrophy.

Pearson PL, van Ommen GJ, Bakker E. Pearson PL, et al. Among authors: bakker e. Cold Spring Harb Symp Quant Biol. 1986;51 Pt 1:353-8. doi: 10.1101/sqb.1986.051.01.042. Cold Spring Harb Symp Quant Biol. 1986. PMID: 2884063 No abstract available.

8

Germline mosaicism and Duchenne muscular dystrophy mutations.

Bakker E, Van Broeckhoven C, Bonten EJ, van de Vooren MJ, Veenema H, Van Hul W, Van Ommen GJ, Vandenberghe A, Pearson PL. Bakker E, et al. Nature. 1987 Oct 8-14;329(6139):554-6. doi: 10.1038/329554a0. Nature. 1987. PMID: 2889144

9

Direct detection of more than 50% of the Duchenne muscular dystrophy mutations by field inversion gels.

den Dunnen JT, Bakker E, Breteler EG, Pearson PL, van Ommen GJ. den Dunnen JT, et al. Among authors: bakker e. Nature. 1987 Oct 15-21;329(6140):640-2. doi: 10.1038/329640a0. Nature. 1987. PMID: 2889148

10

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. Among authors: bakker e. Genomics. 1988 Feb;2(2):101-8. doi: 10.1016/0888-7543(88)90090-0. Genomics. 1988. PMID: 2900805

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