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scopus: 14028184000

Hochstenbach, R.

( R. Hochstenbach)


chromosome author manuscript patient j med genet nih-pa duplication diaphragmatic hernia translocation trisomy genet pmc 2006 pubmed author manuscript trisomy 11 q syndrome region diaphragmatic 21. klaassens nih-pa author manuscript hernia klaassen analysis abnormality anomaly patient 1 patient 2 duplication 11 q chromosomal 23.3 mother deletion material 21. breakpoint phenotype feature defect result signal chromosome 11 material g-banded chromosome analysis grant genomic hybridization dysmorphic features baylor college erasmus mc chromosomes 11 birth − − hybridization family clone department netherland genetic airway cytogenetic baylor report family members chromosome 22 material bac clones grant number deletion 12 q chromosomal abnormalities development member airway malformations california santa cruz chromosome 11 q table blood lymphocytes chromosome 12 ~19 mb duplication dysmorphic individual 11 q 23.3-qter cytogenetic analysis rotterdam




1 Most Recent Publications

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