Phenotypic Overlap of Roberts and Baller-Gerold Syndromes in Two Patients With Craniosynostosis, Limb Reductions, and ESCO2 Mutations

Overview of attention for article published in Frontiers in Pediatrics, May 2019

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#Exome sequencing identifies ESCO2 #mutations https://t.co/xBGckppHWH in patients with phenotypic overlap of Roberts and Baller-Gerold #syndromes #craniosynostosis, limb reductions https://t.co/02VsoBfDdD

19 Jun 2019

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Phenotypic Overlap of Roberts and Baller-Gerold Syndromes in Two Patients With Craniosynostosis, Limb Reductions, and ESCO2 Mutations. https://t.co/e4U0BB93eC

14 Jun 2019

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New Research: Phenotypic Overlap of Roberts and Baller-Gerold Syndromes in Two Patients With Craniosynostosis, Limb Reductions, and ESCO2 Mutations: Baller-Gerold (BGS, MIM#218600) and Roberts (RBS, MIM#268300) syndromes are rare autosomal… https://t.co/0B

28 May 2019

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