den Dunnen JT - Search Results

1

High-resolution melting analysis (HRMA): more than just sequence variant screening.

Vossen RH, Aten E, Roos A, den Dunnen JT. Vossen RH, et al. Among authors: den dunnen jt. Hum Mutat. 2009 Jun;30(6):860-6. doi: 10.1002/humu.21019. Hum Mutat. 2009. PMID: 19418555 Review.

2

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

3

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: den dunnen jt. 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.

4

The protein truncation test: A review.

Den Dunnen JT, Van Ommen GJ. Den Dunnen JT, et al. Hum Mutat. 1999;14(2):95-102. doi: 10.1002/(SICI)1098-1004(1999)14:2<95::AID-HUMU1>3.0.CO;2-G. Hum Mutat. 1999. PMID: 10425032 Review.

5

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

6

Nomenclature for the description of human sequence variations.

den Dunnen JT, Antonarakis SE. den Dunnen JT, et al. Hum Genet. 2001 Jul;109(1):121-4. doi: 10.1007/s004390100505. Hum Genet. 2001. PMID: 11479744

7

DGGE-based whole-gene mutation scanning of the dystrophin gene in Duchenne and Becker muscular dystrophy patients.

Hofstra RM, Mulder IM, Vossen R, de Koning-Gans PA, Kraak M, Ginjaar IB, van der Hout AH, Bakker E, Buys CH, van Ommen GJ, van Essen AJ, den Dunnen JT. Hofstra RM, et al. Among authors: den dunnen jt. Hum Mutat. 2004 Jan;23(1):57-66. doi: 10.1002/humu.10283. Hum Mutat. 2004. PMID: 14695533

8

Two-color multiplex ligation-dependent probe amplification: detecting genomic rearrangements in hereditary multiple exostoses.

White SJ, Vink GR, Kriek M, Wuyts W, Schouten J, Bakker B, Breuning MH, den Dunnen JT. White SJ, et al. Among authors: den dunnen jt. Hum Mutat. 2004 Jul;24(1):86-92. doi: 10.1002/humu.20054. Hum Mutat. 2004. PMID: 15221792

9

Targeted exon skipping in transgenic hDMD mice: A model for direct preclinical screening of human-specific antisense oligonucleotides.

Bremmer-Bout M, Aartsma-Rus A, de Meijer EJ, Kaman WE, Janson AA, Vossen RH, van Ommen GJ, den Dunnen JT, van Deutekom JC. Bremmer-Bout M, et al. Among authors: den dunnen jt. Mol Ther. 2004 Aug;10(2):232-40. doi: 10.1016/j.ymthe.2004.05.031. Mol Ther. 2004. PMID: 15294170 Free article.

10

Sarcoglycanopathies and the risk of undetected deletion alleles in diagnosis.

White SJ, Uitte de Willige S, Verbove D, Politano L, Ginjaar I, Breuning MH, den Dunnen JT. White SJ, et al. Among authors: den dunnen jt. Hum Mutat. 2005 Jul;26(1):59. doi: 10.1002/humu.9347. Hum Mutat. 2005. PMID: 15954112

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