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letter . 2005 Aug;42(8):656–662. doi: 10.1136/jmg.2004.027888
Familial scaphocephaly syndrome caused by a novel mutation in the FGFR2 tyrosine kinase domain
G McGillivray
, R Savarirayan
, T Cox
, C Stojkoski
, R McNeil
, A Bankier
, J Bateman
, T Roscioli
, R Gardner
, S Lamande
G McGillivray
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R Savarirayan
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T Cox
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C Stojkoski
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R McNeil
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A Bankier
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J Bateman
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T Roscioli
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R Gardner
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S Lamande
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PMCID: PMC1736114 PMID: 16061565