Mutation c.943G>T (p.Ala315Ser) in FGFR2 Causing a Mild Phenotype of Crouzon Craniofacial Dysostosis in a Three-Generation Family

Overview of attention for article published in Molecular Syndromology, January 2017

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Genetic heterogeneity: Crouzon sdr w/o craniosynostosis due to c.943G>T p.Ala315Ser FGFR2 mut @KargerPublisher https://t.co/Rr2THHYS5x https://t.co/58BLU2wO3Q

RT @Pedia_Team: Is this an individual with a mild Crouzon phenotype? Either do time consuming research (https://t.co/96smEegI4p) or simply…

RT @Pedia_Team: Is this an individual with a mild Crouzon phenotype? Either do time consuming research (https://t.co/96smEegI4p) or simply…

RT @Pedia_Team: Is this an individual with a mild Crouzon phenotype? Either do time consuming research (https://t.co/96smEegI4p) or simply…

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