Adelaide Research & Scholarship
Please use this identifier to cite or link to this item:
https://hdl.handle.net/2440/27529
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| Type: | Journal article |
| Title: | Familial scaphocephaly syndrome caused by a novel mutation in the FGFR2 tyrosine kinase domain |
| Author: | McGillivray, George Savarirayan, Ravi Cox, Timothy Chilton Stojkoski, Cvetan McNeil, R. Bankier, Agnes Bateman, John Francis Roscioli, T. McKinlay Gardner, R. J. Lamade, S. R. |
| Citation: | Journal of Medical Genetics, 2005; 42:656-662 |
| Publisher: | BMJ Publishing Group Ltd. |
| Issue Date: | 2005 |
| ISSN: | 0022-2593 |
| School/Discipline: | School of Molecular and Biomedical Science |
| Statement of Responsibility: | G McGillivray, R Savarirayan, T C Cox, C Stojkoski, R McNeil, A Bankier, J F Bateman, T Roscioli, R J M Gardner, S R Lamandé |
| Keywords: | FGFR2; craniosynostosis; mutation; tyrosine kinase |
| Description: | Copyright © 2005 by the BMJ Publishing Group Ltd. |
| DOI: | 10.1136/jmg.2004.027888 |
| Appears in Collections: | Molecular and Biomedical Science publications |
Files in This Item:
| File | Size | Format | |
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| hdl_27529.pdf | 407.59 kB | Publisher's PDF | View/Open |
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