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KMID : 0367420000430071006
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Journal of Korean Pediatric Society
2000 Volume.43 No. 7 p.1006 ~ p.1011
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A Case of Apert's Syndrome(Acrocophalosyndactyly) with Fibroblast Growth Factor Receptor 2 Exon Ⅲa Mutation
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김형수/Hyung Su Kim
양필순/강지연/김옥영/구철회/이화모/Pyl Soon Yang/Jee Yeoun Kang/Ok Young Kim/Chul Hae Ku/Wha Mo Lee
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Abstract
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KEYWORD
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Apert Syndrome, Acrocephalosyndactyly, Fibroblast growth factor receptor 2 gene (FGFR2),
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