Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome - Concepedia

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Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome

925

Citations

64

References

1995

Year

Andrew O.M. Wilkie, Sarah F. Slaney, Michael Oldridge, Michael D. Poole, Geraldine J. Ashworth, Anthony D. Hockley, Richard Hayward, David J. David, Louise J. Pulleyn, Paul Rutland,

Nature Genetics

Mendelian DisorderAutoimmune DiseaseGenetic DisorderGeneticsGenetic EpidemiologyApert Syndrome ResultsPathologyCraniofacial DevelopmentLocalized MutationsMolecular GeneticsMedicineCrouzon Syndrome

References

	Year	Citations

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