Klaassens, M.

patient diaphragmatic hernia chromosome deletion diaphragmatic hernia anomaly genet defect region syndrome development diaphragm duplication study candidate chromosomal analysis factor j med genet translocation result birth model chapter klaassen feature coup-tfii abnormality retinoic animal models signal number retinoic acid lung development mutation trisomy chromosomal anomalies phenotype candidate genes etiology figure animal diaphragm development children ea /tef diagn probe pathway cause genomic array family dysmorphic features chromosome 15 q candidate region research change fryns syndrome table prenat hybridization group genomic hybridization receptor cdh patients expression 15 q 26 g-banded chromosome analysis patient 1 15 q deletion cytogenetic diaphragm defects clone dysmorphic author tibboel appendix manuscript array-cgh