Research Topics
| M KlaassensSummaryAffiliation: Erasmus MC Country: The Netherlands Publications
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Detail Information
Publications
Congenital diaphragmatic hernia associated with duplication of 11q23-qterM Klaassens
Department of Clinical Genetics, Erasmus MC, Rotterdam, The Netherlands
Am J Med Genet A 140:1580-6. 2006..We also conclude that the partial trisomy 11q syndrome has a variable phenotype and that CDH should be added to the spectrum of anomalies that can be present in this syndrome...
Congenital diaphragmatic hernia and chromosome 15q26: determination of a candidate region by use of fluorescent in situ hybridization and array-based comparative genomic hybridizationM Klaassens
Department of Paediatric Surgery, Erasmus Medical Centre, Rotterdam, The Netherlands
Am J Hum Genet 76:877-82. 2005..1-26.2. The region contains four known genes, of which two--NR2F2 and CHD2--are particularly intriguing gene candidates for CDH...
Prenatal detection and outcome of congenital diaphragmatic hernia (CDH) associated with deletion of chromosome 15q26: two patients and review of the literatureM Klaassens
Department of Clinical Genetics, Erasmus MC, Rotterdam, The Netherlands
Am J Med Genet A 143:2204-12. 2007....
The etiology of congenital diaphragmatic hernia: still largely unknown?M Klaassens
Department of Pediatric Surgery, Erasmus MC, Medical University Center, room Ee9 71, PO Box 2040, 3000 CA Rotterdam, The Netherlands
Eur J Med Genet 52:281-6. 2009..We also propose a protocol for the CDH patient that will help clinicians and researchers to obtain maximal success out of their collaborations that will eventually lead to unravelling the etiology of this intriguing birth defect...
Genetic factors in congenital diaphragmatic herniaA M Holder
Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA
Am J Hum Genet 80:825-45. 2007....
