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Familial scaphocephaly syndrome caused by a novel mutation in the FGFR2 tyrosine kinase domain
- Correspondence to: Dr Shireen R Lamandé Murdoch Childrens Research Institute, Royal Children’s Hospital, Parkville 3052, Victoria, Australia; shireen.lamandemcri.edu.au
Citation
Familial scaphocephaly syndrome caused by a novel mutation in the FGFR2 tyrosine kinase domain
Publication history
- Received October 6, 2004
- Accepted December 21, 2004
- Revised December 13, 2004
- First published August 1, 2005.
Online issue publication
April 27, 2016
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Copyright 2005 Journal of Medical Genetics