Publications 2004

Genome-wide array-based comparative genomic hybridization reveals multiple amplification targets and novel homozygous deletions in pancreatic carcinoma cell lines. Heidenblad M, Schoenmakers EF, Jonson T, Gorunova L, Veltman JA, Geurts van Kessel A, and Hoglund M.
Cancer Res., 64: 3052-3059 (2004).


Loss of a small region around the PTEN locus is a major chromosome 10 alteration in prostate cancer xenografts and cell lines. Hermans KG, van Alewijk DC, Veltman JA, van Weerden W, Geurts van Kessel A, and Trapman J.
Genes Chromosomes Cancer, 39: 171-184 (2004).


A novel microdeletion, del(2)(q22.3q23.3) in a mentally retarded patient, detected by array-based comparative genomic hybridization. Koolen DA, Vissers LE, Nillesen W, Smeets D, van Ravenswaaij CM, Sistermans EA, Veltman JA, and de Vries BB.
Clin.Genet., 65: 429-432 (2004).


Chromosome 22q11 deletion and pachygyria characterized by array-based comparative genomic hybridization. Koolen DA, Veltman JA, Renier WO, Droog RP, Geruts van Kessel A, and de Vries BB.
Am.J.Med.Genet.A, 131: 322-324 (2004).


High resolution profiling of X chromosomal aberrations by array comparative genomic hybridisation. Veltman JA, Yntema HG, Lugtenberg D, Arts H, Briault S, Huys EH, Osoegawa K, de Jong P, Brunner HG, Geurts van Kessel A, van BH, and Schoenmakers EF.
J.Med.Genet., 41: 425-432 (2004).


Mutations in a new member of the chromodomain gene family cause CHARGE syndrome. Vissers LE, van Ravenswaaij CM, Admiraal R, Hurst JA, de Vries BB, Janssen IM, van der Vliet W, Huys EH, de Jong PJ, Hamel BC, Schoenmakers EF, Brunner HG, Veltman JA, and Geurts van Kessel A.
Nat.Genet., 36: 955-957 (2004).