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scopus: 7006029996

Wouters, C.

(Cokkie Wouters)


patient chromosome diaphragmatic hernia deletion syndrome author manuscript abnormality genet region hybridization anomaly genomic hybridization analysis diaphragmatic j med genet chromosomal nih-pa translocation material hernia genomic trisomy study duplication defect signal result pmc 2006 pubmed author manuscript trisomy 11 q chromosomal abnormalities feature netherland probe cytogenetic dysmorphic features karyotype department culture autopsy clone 21. klaassens nih-pa author manuscript chromosome 15 q iugr dysmorphic features tissue array cgh system erasmus mc cytogenetic analysis technique klaassen array table dysmorphic bac clones development cdh region patient 1 patient 2 duplication 11 q 23.3 15 q deletions mother erasmu paraffin-embedded metaphase report 21. breakpoint phenotype member cgh analysis genome rotterdam diaphragmatic defects paraffin-embedded autopsy material chromosome 11 material




3 Most Recent Publications

The use of comparative genomic hybridization and fluorescent in situ hybridization in postmortem pathology investigation of congenital malformations (Article)
Goemaere, N.N.T. Douben, H. Opstal, D. van Wouters, C. Tibboel, D. Krijger, R.R. de Klein, J.E.M.M. de
2010-03-01
Congenital diaphragmatic hernia associated with duplication of 11q23-qter. (Article)
Klaassens, M. Scott, D.A. Lee, B. Tibboel, D. Klein, J.E.M.M. de Dooren, M.F. van Hochstenbach, R. Eussen, B.H.J. Cai, W.W. Galjaard, R-J.H. Wouters, C. Poot, M. Laudij, J.A.M.
2006-07-15
Congenital diaphragmatic hernia and chromosome 15q26: determination of a candidate region by use of fluorescent in situ hybridization and array-based comparative genomic hybridization (Article)
Klaassens, M. Wouters, C. Galjaard, R-J.H. Goemaere, N.N.T. Oostra, B.A. Krijger, R.R. de Wauters, J. Dooren, M.F. van Eussen, B.H.J. Douben, H. Klein, J.E.M.M. de Dekker, A.T. den Lee, C. Donahoe, P.K. Tibboel, D.
2005-01-01