• <em>SLC25A24</em> Fontaine Progeroid Syndrome
• A 9-year-old Korean girl with Fontaine progeroid syndrome: a case report with further phenotypical delineation and description of clinical course during long-term follow-up
• A high-resolution daily global dataset of statistically downscaled CMIP6 models for climate impact analyses
• A rare male patient with Fontaine progeroid syndrome caused by p.R217H de novo mutation in SLC25A24
• Absence of nasal bone and brachydactyly: a probable new familial syndrome
• Accurate Detection of Dysmorphic Nuclei Using Dynamic Programming and Supervised Classification
• An etiologic and nosologic overview of craniosynostosis syndromes
• Benefit of piezoosteotomy in cranioplasties for craniosynostosis correction versus conventional saw-and-chisel osteotomy: a pilot study
• Craniofacial dysostosis, hypertrichosis, genital hypoplasia, ocular, dental, and digital defects: confirmation of the Gorlin-Chaudhry-Moss syndrome
• Craniofacial dysostosis, patent ductus arteriosus, hypertrichosis, hypoplasia of labia majora, dental and eye anomalies-a new syndrome?
• De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction
• Different GCMs yet similar outcome: predicting the habitat distribution of Shorea robusta C.F. Gaertn. in the Indian Himalayas using CMIP5 and CMIP6 climate models
• Gorlin-Chaudhry-Moss or Saethre-Chotzen syndrome?
• Gorlin-Chaudhry-Moss syndrome
• Gorlin-Chaudhry-Moss syndrome revisited: expanding the phenotype
• Is Gorlin-Chaudhry-Moss syndrome associated with aortopathy?
• Necrotizing soft tissue infection of the scalp after fronto-facial advancement by internal distraction in a 7-year old girl with Gorlin-Chaudhry-Moss syndrome--a case report
• Oculo-facio-cardio-dental syndrome with craniosynostosis, temporal hypertrichosis, and deafness
• Performance evaluation of CMIP6 climate models for selecting a suitable GCM for future precipitation at different places of Tamil Nadu
• Two sisters resembling Gorlin-Chaudhry-Moss syndrome