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
Guardado en:
| Autores principales: | , , |
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| Otros Autores: | , , , , , , , , , , , , , , , , , , , , , |
| Formato: | Article (Journal) |
| Lenguaje: | inglés |
| Publicado: |
December 2013
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| In: |
American journal of medical genetics
Year: 2013, Volumen: 161, Número: 12, Pages: 3035-3041 |
| ISSN: | 1552-4833 |
| Acceso en línea: | Verlag, Abstract, Volltext: http://onlinelibrary.wiley.com/doi/10.1002/ajmg.a.36153/abstract |
| Notas de Autor: | 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 |
| Descripción Física: | Online Resource |
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| ISSN: | 1552-4833 |