High frequency of p.Thr93Met in Smith-Lemli-Opitz syndrome patients in Turkey
Gespeichert in:
| Hauptverfasser: | , |
|---|---|
| Dokumenttyp: | Article (Journal) Editorial |
| Sprache: | Englisch |
| Veröffentlicht: |
2012
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| In: |
Clinical genetics
Year: 2011, Jahrgang: 81, Heft: 6, Pages: 598-601 |
| ISSN: | 1399-0004 |
| DOI: | 10.1111/j.1399-0004.2011.01750.x |
| Online-Zugang: | Verlag, Volltext: http://dx.doi.org/10.1111/j.1399-0004.2011.01750.x Verlag, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1111/j.1399-0004.2011.01750.x 
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| Verfasserangaben: | S. Kalb, A.O. Caglayan, A. Degerliyurt, S. Schmid, S. Ceylaner, N. Hatipoglu, K. Hinderhofer, H. Rehder, S. Kurtoglu, G. Ceylaner, J. Zschocke, M. Witsch‐Baumgartner |
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