Disease: Cutis Gyrata syndrome of Beare and Stevenson
- A Case of Beare-Stevenson Syndrome with Unusual Manifestations
- Atypical Skin Manifestations in <em>FGFR2</em>-Related Craniosynostosis Syndromes Broaden the Phenotypic Spectrum
- Beare-Stevenson Syndrome With Blepharoptosis as a Complication of Front-Orbital Advancement and Remodeling
- Beare-Stevenson syndrome: two Dutch patients with cerebral abnormalities
- Beare-Stevenson syndrome: two new patients, including a novel finding of tracheal cartilaginous sleeve
- Cerebriform sebaceous nevus: a subtype of organoid nevus due to specific postzygotic FGFR2 mutations
- Clinicogenetic study of Turkish patients with syndromic craniosynostosis and literature review
- Fibroblast Growth Factor Receptor 2 (<em>FGFR2</em>) Mutation Related Syndromic Craniosynostosis
- Fibroblast growth factor receptor signaling in kidney and lower urinary tract development
- Genotype-Phenotype Correlation of Tracheal Cartilaginous Sleeves and Fgfr2 Mutations in Mice
- Hearing loss in syndromic craniosynostoses: otologic manifestations and clinical findings
- p38 Inhibition ameliorates skin and skull abnormalities in Fgfr2 Beare-Stevenson mice
- Posterior Distraction First or Fronto-Orbital Advancement First for Severe Syndromic Craniosynostosis
- The effect of a Beare-Stevenson syndrome Fgfr2 Y394C mutation on early craniofacial bone volume and relative bone mineral density in mice
- Tracheal cartilaginous sleeve in patients with Beare-Stevenson syndrome