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High frequency of p.Thr93Met in Smith-Lemli-Opitz syndrome patients in Turkey

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Bibliographic Details
Main Authors: Kalb, Stefanie (Author) , Hinderhofer, Katrin (Author)
Format: Article (Journal) Editorial
Language:English
Published: 2012
In: Clinical genetics
Year: 2011, Volume: 81, Issue: 6, Pages: 598-601
ISSN:1399-0004
DOI:10.1111/j.1399-0004.2011.01750.x
Online Access: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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Author Notes: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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Item Description:First published: 28 December 2011
Gesehen am 14.07.2018
Physical Description:Online Resource
ISSN:1399-0004
DOI:10.1111/j.1399-0004.2011.01750.x

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