Heterozygous FGF8 mutations in patients presenting cryptorchidism and multiple VATER/VACTERL features without limb anomalies
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| Main Authors: | , , |
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| Other Authors: | , , , , , , , , , , , , , , , , , , , , , , |
| Format: | Article (Journal) |
| Language: | English |
| Published: |
8 August 2014
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| In: |
Birth defects research. Part A, Clinical and molecular teratology
Year: 2014, Volume: 100, Issue: 10, Pages: 750-759 |
| ISSN: | 1542-0760 |
| DOI: | 10.1002/bdra.23278 |
| Online Access: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1002/bdra.23278 Verlag, Abstract, Volltext: http://onlinelibrary.wiley.com/doi/10.1002/bdra.23278/abstract |
| Author Notes: | 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 |
| Item Description: | Gesehen am 15.07.2020 |
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| Physical Description: | Online Resource |
| ISSN: | 1542-0760 |
| DOI: | 10.1002/bdra.23278 |