1. Clinical assessment and FGFR2 mutation analysis in a Chinese family with Crouzon syndrome
   Huijun Shi et al, 2021, Medicine CrossRef
2. Identification of Diagnostic Variants in FGFR2 and NPR2 Genes in a Chinese Family Affected by Crouzon Syndrome and Acromesomelic Dysplasia, Type Maroteaux
   JianJiang Zhu et al, 2022, DNA and Cell Biology CrossRef
3. Crouzon syndrome in a fraternal twin: A case report and review of the literature
   Xiao-Jing Li et al, 2022, World Journal of Clinical Cases CrossRef
4. Genetic variations in Bestrophin‑1 and associated clinical findings in two Chinese patients with juvenile‑onset and adult‑onset best vitelliform macular dystrophy
   Ying Lin et al, 2017, Molecular Medicine Reports CrossRef
5. Severe Cloverleaf Skull Deformity in c.1061C>G (p.Ser354Cys) Mutated Fibroblast Growth Factor Receptor 2 Gene in Crouzon Syndrome
   Sarut Chaisrisawadisuk et al, 2021, Journal of Craniofacial Surgery CrossRef
6. A novel p.Pro871Leu missense mutation in SPECC1L gene causing craniosynostosis in a patient
   Shanshan Bai et al, 2021, Orthodontics & Craniofacial Research CrossRef
7. Genética‌‌ de‌‌ las‌‌ fisuras‌‌ labiopalatinas‌‌:‌ una‌‌ visión‌ general‌‌ de‌‌ los‌‌ factores‌‌ de‌‌ riesgo‌‌ genéticos‌‌ y‌‌ ambientales
   Daniela Estefania Pusapaz Pusapaz et al, 2022, Revista Med CrossRef
8. FGFR2 Mutation p.Cys342Arg Enhances Mitochondrial Metabolism-Mediated Osteogenesis via FGF/FGFR-AMPK-Erk1/2 Axis in Crouzon Syndrome
   Yidi Wang et al, 2022, Cells CrossRef
9. Detection of G338R FGFR2 mutation in a Vietnamese patient with Crouzon syndrome
   Anh Luong et al, 2019, Biomedical Reports CrossRef
10. Targeted next‑generation sequencing identifies two novel COL2A1 gene mutations in Stickler syndrome with bilateral retinal detachment
    Xinhua Huang et al, 2018, International Journal of Molecular Medicine CrossRef