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- W2083816665 abstract "We report a baby with craniosynostosis and a sacral appendage who has been found to have a Ser351Cys mutation in the fibroblast growth factor receptor 2 gene (FGFR2). This is the first report of sacral appendage associated with a confirmed mutation in one of the FGFR genes, and adds to the spectrum of abnormalities which can be seen in patients with FGFR mutations." @default.
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- W2083816665 date "2002-07-01" @default.
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- W2083816665 title "Sacral appendage associated with a mutation in FGFR2" @default.
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- W2083816665 doi "https://doi.org/10.1097/00019605-200207000-00016" @default.
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