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Congenital diaphragmatic hernia and a complex heart defect in association with Wolf–Hirschhorn syndrome

2010; Wiley; Volume: 152A; Issue: 11 Linguagem: Inglês

10.1002/ajmg.a.33660

1552-4833

Juliane Tautz, Danielle Veenma, Bert Eussen, Linda Joosen, Pino J. Poddighe, Dick Tibboel, Annelies de Klein, Thomas Schaible,

Tracheal and airway disorders

American Journal of Medical Genetics Part AVolume 152A, Issue 11 p. 2891-2894 Research Letter Congenital diaphragmatic hernia and a complex heart defect in association with Wolf–Hirschhorn syndrome†‡ Juliane Tautz, Juliane Tautz Universitatsklinikum Mannheim, Paediatric Intensive Care Unit, Mannheim, Germany Juliane Tautz and Danielle Veenma contributed equally to this work.Search for more papers by this authorDanielle Veenma, Corresponding Author Danielle Veenma [email protected] Erasmus MC Rotterdam, Pediatric Surgery Department, Rotterdam, the Netherlands Erasmus MC Rotterdam, Clinical Genetic Department, Rotterdam, the Netherlands Juliane Tautz and Danielle Veenma contributed equally to this work.Department of Clinical Genetics, Rm Ee 971, PO Box 2040, 3000 CA Rotterdam, the Netherlands.Search for more papers by this authorBert Eussen, Bert Eussen Erasmus MC Rotterdam, Clinical Genetic Department, Rotterdam, the NetherlandsSearch for more papers by this authorLinda Joosen, Linda Joosen Erasmus MC Rotterdam, Clinical Genetic Department, Rotterdam, the NetherlandsSearch for more papers by this authorPino Poddighe, Pino Poddighe Erasmus MC Rotterdam, Clinical Genetic Department, Rotterdam, the NetherlandsSearch for more papers by this authorDick Tibboel, Dick Tibboel Erasmus MC Rotterdam, Pediatric Surgery Department, Rotterdam, the NetherlandsSearch for more papers by this authorAnnelies de Klein, Annelies de Klein Erasmus MC Rotterdam, Clinical Genetic Department, Rotterdam, the NetherlandsSearch for more papers by this authorThomas Schaible, Thomas Schaible Universitatsklinikum Mannheim, Paediatric Intensive Care Unit, Mannheim, GermanySearch for more papers by this author Juliane Tautz, Juliane Tautz Universitatsklinikum Mannheim, Paediatric Intensive Care Unit, Mannheim, Germany Juliane Tautz and Danielle Veenma contributed equally to this work.Search for more papers by this authorDanielle Veenma, Corresponding Author Danielle Veenma [email protected] Erasmus MC Rotterdam, Pediatric Surgery Department, Rotterdam, the Netherlands Erasmus MC Rotterdam, Clinical Genetic Department, Rotterdam, the Netherlands Juliane Tautz and Danielle Veenma contributed equally to this work.Department of Clinical Genetics, Rm Ee 971, PO Box 2040, 3000 CA Rotterdam, the Netherlands.Search for more papers by this authorBert Eussen, Bert Eussen Erasmus MC Rotterdam, Clinical Genetic Department, Rotterdam, the NetherlandsSearch for more papers by this authorLinda Joosen, Linda Joosen Erasmus MC Rotterdam, Clinical Genetic Department, Rotterdam, the NetherlandsSearch for more papers by this authorPino Poddighe, Pino Poddighe Erasmus MC Rotterdam, Clinical Genetic Department, Rotterdam, the NetherlandsSearch for more papers by this authorDick Tibboel, Dick Tibboel Erasmus MC Rotterdam, Pediatric Surgery Department, Rotterdam, the NetherlandsSearch for more papers by this authorAnnelies de Klein, Annelies de Klein Erasmus MC Rotterdam, Clinical Genetic Department, Rotterdam, the NetherlandsSearch for more papers by this authorThomas Schaible, Thomas Schaible Universitatsklinikum Mannheim, Paediatric Intensive Care Unit, Mannheim, GermanySearch for more papers by this author First published: 09 September 2010 https://doi.org/10.1002/ajmg.a.33660Citations: 12 † There are no competing interests. ‡ How to Cite this Article: Tautz J, Veenma D, Eussen B, Joosen L, Poddighe P, Tibboel D, de Klein A, Schaible T. 2010. 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