Integrating imaging and genomics in prenatal Treacher Collins syndrome: evidence for practice and policy
- DOI
- 10.1186/s13023-025-04094-4
- Published
- 2026-03-19
- 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/s13023-025-04094-4,
title = {Integrating imaging and genomics in prenatal Treacher Collins syndrome: evidence for practice and policy},
author = {Chunling Li and Wei Huang and Zhongzhi Gan and Yin Ling and Liyan Qiu and Yuanling Xiao and Fu Xiong and Fang Yang},
year = {2026},
journal = {Orphanet Journal of Rare Diseases},
doi = {10.1186/s13023-025-04094-4},
url = {https://doi.org/10.1186/s13023-025-04094-4}
}RIS
TY - JOUR TI - Integrating imaging and genomics in prenatal Treacher Collins syndrome: evidence for practice and policy AU - Chunling Li AU - Wei Huang AU - Zhongzhi Gan AU - Yin Ling AU - Liyan Qiu AU - Yuanling Xiao AU - Fu Xiong AU - Fang Yang PY - 2026 JO - Orphanet Journal of Rare Diseases DO - 10.1186/s13023-025-04094-4 UR - https://doi.org/10.1186/s13023-025-04094-4 ER -
APA
Li, C., Huang, W., Gan, Z., Ling, Y., Qiu, L., Xiao, Y., Xiong, F., & Yang, F. (2026). Integrating imaging and genomics in prenatal Treacher Collins syndrome: evidence for practice and policy. Orphanet Journal of Rare Diseases. https://doi.org/10.1186/s13023-025-04094-4
Source records
- crossref · retrieved 2026-11-10T14:21:52.692Z