Closing the Gap: Genetic and Genomic Continuum from Syndromic to Nonsyndromic Craniosynostoses

Míreanna comhchosúla

• Closing the Gap: Genetic and Genomic Continuum from Syndromic to Nonsyndromic Craniosynostoses
  de réir: Heuzé, Yann, et al.
  Foilsithe / Cruthaithe: (2014)
• Mutation Screening of Candidate Genes in Patients with Nonsyndromic Sagittal Craniosynostosis
  de réir: Ye, Xiaoqian, et al.
  Foilsithe / Cruthaithe: (2016)
• Nonsyndromic Craniosynostosis: Novel Coding Variants
  de réir: Sewda, Anshuman, et al.
  Foilsithe / Cruthaithe: (2019)
• Morphological comparison of the craniofacial phenotypes of mouse models expressing the Apert FGFR2 S252W mutation in neural crest- or mesoderm-derived tissues
  de réir: Heuzé, Yann, et al.
  Foilsithe / Cruthaithe: (2014)
• FGF/FGFR Signaling Coordinates Skull Development by Modulating Magnitude of Morphological Integration: Evidence from Apert Syndrome Mouse Models
  de réir: Martínez-Abadías, Neus, et al.
  Foilsithe / Cruthaithe: (2011)