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A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) causes non-syndromic craniosynostosis

โœ Scribed by F-J Tsai; J-Y Wu; C-C Lee; C-H Tsai

Book ID
114812426
Publisher
John Wiley and Sons
Year
2000
Tongue
English
Weight
60 KB
Volume
89
Category
Article
ISSN
0803-5253

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