De novo 13q deletions in two patients with mild anorectal malformations as part of VATER/VACTERL and VATER/VACTERL-like association and analysis of EFNB2 in patients with anorectal malformations
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| Hauptverfasser: | , , |
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| Weitere Verfasser: | , , , , , , , , , , , , , , , , , , , , , |
| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
December 2013
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| In: |
American journal of medical genetics
Year: 2013, Jahrgang: 161, Heft: 12, Pages: 3035-3041 |
| ISSN: | 1552-4833 |
| Online-Zugang: | Verlag, Abstract, Volltext: http://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.36153/abstract
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| Verfasserangaben: | Gabriel C. Dworschak, Markus Draaken, Carlo Marcelis, Ivo de Blaauw, Rolph Pfundt, Iris A.L.M. van Rooij, Enrika Bartels, Alina Hilger, Ekkehart Jenetzky, Eberhard Schmiedeke, Sabine Grasshoff-Derr, Dominik Schmidt, Stefanie Märzheuser, Stuart Hosie, Sandra Weih, Stefan Holland-Cunz, Markus Palta, Johannes Leonhardt, Mattias Schäfer, Christina Kujath, Anke Rißmann, Markus M. Nöthen, Nadine Zwink, Michael Ludwig, and Heiko Reutter |
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