Klein, J.E.M.M. de

chromosome patient melanoma analysis region tumor expression study deletion diaphragmatic hernia genet uveal mutation syndrome uveal melanoma probe anomaly diaphragmatic protein result chromosomal development cancer defect hernia number factor sample genomic children abnormality control sequence level identi ea /tef duplication cytogenetic figure survival table identi fied research netherland pathway cell lines model array atresia hybridization chromosome 3 effect diaphragm translocation folate breakpoint signi change genetic disease fication trisomy signal rotterdam association phenotype monosomy tissue ratio birth pediatr erasmus mc j med genet family prognostic feature aberration genome journal esophageal atresia