Publication | Open Access
Genomic Screening of Fibroblast Growth-Factor Receptor 2 Reveals a Wide Spectrum of Mutations in Patients with Syndromic Craniosynostosis
264
Citations
71
References
2002
Year
SclerostinDevelopmental BiologyMendelian DisorderSyndromic CraniosynostosisWide SpectrumCraniofacial DevelopmentFibroblast Growth FactorNeurogeneticsMedicineCell BiologyCraniofacial DisorderGenomic ScreeningMolecular Medicine
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