Diagnosis of rare diseases based on facial phenotype: a quantitative assessment using 2D and 3D photography in Stickler syndrome
- DOI
- 10.1186/s13023-026-04323-4
- Published
- 2026-07-27
- Container
- Orphanet Journal of Rare Diseases
- Publisher
- Springer Science and Business Media LLC
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1186/s13023-026-04323-4,
title = {Diagnosis of rare diseases based on facial phenotype: a quantitative assessment using 2D and 3D photography in Stickler syndrome},
author = {Adèle Rohée-Traoré and Maxime Taverne and Quentin Hennocq and Thomas Bongibault and Alejandra Daruich and Dominique Bremond-Gignac and Jean-Daniel Kün-Darbois and Pierre-Raphaël Rothschild and Roman-Hossein Khonsari},
year = {2026},
journal = {Orphanet Journal of Rare Diseases},
doi = {10.1186/s13023-026-04323-4},
url = {https://doi.org/10.1186/s13023-026-04323-4}
}RIS
TY - JOUR TI - Diagnosis of rare diseases based on facial phenotype: a quantitative assessment using 2D and 3D photography in Stickler syndrome AU - Adèle Rohée-Traoré AU - Maxime Taverne AU - Quentin Hennocq AU - Thomas Bongibault AU - Alejandra Daruich AU - Dominique Bremond-Gignac AU - Jean-Daniel Kün-Darbois AU - Pierre-Raphaël Rothschild AU - Roman-Hossein Khonsari PY - 2026 JO - Orphanet Journal of Rare Diseases DO - 10.1186/s13023-026-04323-4 UR - https://doi.org/10.1186/s13023-026-04323-4 ER -
APA
Rohée-Traoré, A., Taverne, M., Hennocq, Q., Bongibault, T., Daruich, A., Bremond-Gignac, D., Kün-Darbois, J., Rothschild, P., & Khonsari, R. (2026). Diagnosis of rare diseases based on facial phenotype: a quantitative assessment using 2D and 3D photography in Stickler syndrome. Orphanet Journal of Rare Diseases. https://doi.org/10.1186/s13023-026-04323-4
Source records
- crossref · retrieved 2026-09-25T16:53:19.636Z