J. Dunnen

发表

The human genome project and the future of diagnostics, treatment, and prevention

E. Bakker, G. V. Ommen, J. D. Dunnen, 1999, The Lancet.

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

P. Pearson, H. Veenema, P. Grootscholten, 1989, Journal of Inherited Metabolic Disease.

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

C. van Broeckhoven, J. D. den Dunnen, M. Wapenaar, 1989, American journal of human genetics.

Muscle regeneration in dystrophin-deficient mdx mice studied by gene expression profiling

P. Hoen, E. Sterrenburg, Rolf Turk, 2005, BMC Genomics.

Application of in vitro myo-differentiation of non-muscle cells to enhance gene expression and facilitate analysis of muscle proteins

G. V. Ommen, R. Hoeben, P. Roest, 1996, Neuromuscular Disorders.

Predicted and observed sizes of dystrophin in some patients with gene deletions that disrupt the open reading frame.

K. Bushby, J. D. den Dunnen, M. Johnson, 1992, Journal of medical genetics.

An alternative to FISH: detecting deletion and duplication carriers within 24 hours

J. D. den Dunnen, S. White, M. Breuning, 2003, Journal of medical genetics.

WHSC1, a 90 kb SET domain-containing gene, expressed in early development and homologous to a Drosophila dysmorphy gene maps in the Wolf-Hirschhorn syndrome critical region and is fused to IgH in t(4;14) multiple myeloma.

A. Moorman, P. D. de Boer, J. T. Dunnen, 1998, Human molecular genetics.

Long-range genomic map of the Duchenne muscular dystrophy (DMD) gene: isolation and use of J66 (DXS268), a distal intragenic marker.

C. Bertelson, L. Kunkel, J. D. den Dunnen, 1987, Genomics.

Genomic imbalances in mental retardation

J. D. den Dunnen, G. V. van Ommen, S. White, 2004, Journal of Medical Genetics.