Persistent URL of this record https://hdl.handle.net/1887/104782
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Homozygous and Compound-Heterozygous Mutations in TGDS Cause Catel-Manzke Syndrome
- All authors
- Ehmke, N.; Caliebe, A.; Koenig, R.; Kant, S.G.; Stark, Z.; Cormier-Daire, V.; Wieczorek, D.; Gillessen-Kaesbach, G.; Hoff, K.; Kawalia, A.; Thiele, H.; Altmuller, J.; Fischer-Zirnsak, B.; Knaus, A.; Zhu, N.; Heinrich, V.; Huber, C.; Harabula, I.; Spielmann, M.; Horn, D.; Komak, U.; Hecht, J.; Krawitz, P.M.; Nurnberg, P.; Siebert, R.; Manzke, H.; Mundlos, S.
- Date
- 2014-12-04
- Volume
- 95
- Issue
- 6
- Pages
- 763 - 770