den Dunnen JT - Search Results

1

Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion.

den Dunnen JT, Antonarakis SE. den Dunnen JT, et al. Hum Mutat. 2000;15(1):7-12. doi: 10.1002/(SICI)1098-1004(200001)15:1<7::AID-HUMU4>3.0.CO;2-N. Hum Mutat. 2000. PMID: 10612815

2

Reconstruction of the 2.4 Mb human DMD-gene by homologous YAC recombination.

Den Dunnen JT, Grootscholten PM, Dauwerse JG, Walker AP, Monaco AP, Butler R, Anand R, Coffey AJ, Bentley DR, Steensma HY, et al. Den Dunnen JT, et al. Hum Mol Genet. 1992 Apr;1(1):19-28. doi: 10.1093/hmg/1.1.19. Hum Mol Genet. 1992. PMID: 1301131

3

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: den dunnen jt. 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.

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

5

Germinal mosaicism increases the recurrence risk for 'new' Duchenne muscular dystrophy mutations.

Bakker E, Veenema H, Den Dunnen JT, van Broeckhoven C, Grootscholten PM, Bonten EJ, van Ommen GJ, Pearson PL. Bakker E, et al. Among authors: den dunnen jt. J Med Genet. 1989 Sep;26(9):553-9. doi: 10.1136/jmg.26.9.553. J Med Genet. 1989. PMID: 2810338 Free PMC article.

6

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. Nature. 1987 Oct 15-21;329(6140):640-2. doi: 10.1038/329640a0. Nature. 1987. PMID: 2889148

7

A provisional transcript map of the spinal muscular atrophy (SMA) critical region.

van der Steege G, Draaijers TG, Grootscholten PM, Osinga J, Anzevino R, Velonà I, Den Dunnen JT, Scheffer H, Brahe C, van Ommen GJ, et al. van der Steege G, et al. Among authors: den dunnen jt. Eur J Hum Genet. 1995;3(2):87-95. doi: 10.1159/000472281. Eur J Hum Genet. 1995. PMID: 7552146

8

Expression of the human Dp 71 (apo-dystrophin-1) gene from a 760-kb DMD-YAC transferred to mouse cells.

Heikoop JC, Hogervorst FB, Meershoek EJ, Grootscholten PM, den Dunnen JT, van Ommen GJ. Heikoop JC, et al. Among authors: den dunnen jt. Eur J Hum Genet. 1995;3(3):168-79. doi: 10.1159/000472292. Eur J Hum Genet. 1995. PMID: 7583042

9

Point mutation screening for 16 exons of the dystrophin gene by multiplex single-strand conformation polymorphism analysis.

Kneppers AL, Deutz-Terlouw PP, den Dunnen JT, van Ommen GJ, Bakker E. Kneppers AL, et al. Among authors: den dunnen jt. Hum Mutat. 1995;5(3):235-42. doi: 10.1002/humu.1380050308. Hum Mutat. 1995. PMID: 7599634

10

High-resolution DNA Fiber-FISH for genomic DNA mapping and colour bar-coding of large genes.

Florijn RJ, Bonden LA, Vrolijk H, Wiegant J, Vaandrager JW, Baas F, den Dunnen JT, Tanke HJ, van Ommen GJ, Raap AK. Florijn RJ, et al. Among authors: den dunnen jt. Hum Mol Genet. 1995 May;4(5):831-6. doi: 10.1093/hmg/4.5.831. Hum Mol Genet. 1995. PMID: 7633442

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