Heterozygous FGF8 mutations in patients presenting cryptorchidism and multiple VATER/VACTERL features without limb anomalies
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| Hauptverfasser: | , , |
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| Weitere Verfasser: | , , , , , , , , , , , , , , , , , , , , , , |
| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
8 August 2014
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| In: |
Birth defects research. Part A, Clinical and molecular teratology
Year: 2014, Jahrgang: 100, Heft: 10, Pages: 750-759 |
| ISSN: | 1542-0760 |
| DOI: | 10.1002/bdra.23278 |
| Online-Zugang: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1002/bdra.23278 Verlag, Abstract, Volltext: http://onlinelibrary.wiley.com/doi/10.1002/bdra.23278/abstract 
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| Verfasserangaben: | Claudia Zeidler, Joachim Woelfle, Markus Draaken, Sadaf S. Mughal, Greta Große,Alina C. Hilger, Gabriel C. Dworschak, Thomas M. Boemers, Ekkehart Jenetzky,Nadine Zwink, Martin Lacher, Dominik Schmidt, Eberhard Schmiedeke,Sabine Grasshoff-Derr, Stefanie Märzheuser, Stefan Holland-Cunz, Mattias Schäfer,Enrika Bartels, Kathleen Keppler, Markus Palta, Johannes Leonhardt, ChristinaKujath, Anke Rißmann, Markus M. Nöthen, Heiko Reutter, and Michael Ludwig |
MARC
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