De novo variants implicate chromatin modification, transcriptional regulation, and retinoic acid signaling in syndromic craniosynostosis.
- DOI
- 10.1016/j.ajhg.2023.03.017
- Published
- 2023 May 4
- Container
- American journal of human genetics
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1016/j.ajhg.2023.03.017,
title = {De novo variants implicate chromatin modification, transcriptional regulation, and retinoic acid signaling in syndromic craniosynostosis.},
author = {Timberlake AT and McGee S and Allington G and Kiziltug E and Wolfe EM and Stiegler AL and Boggon TJ and Sanyoura M and Morrow M and Wenger TL and Fernandes EM and Caluseriu O and Persing JA and Jin SC and Lifton RP and Kahle KT and Kruszka P},
year = {2023},
journal = {American journal of human genetics},
doi = {10.1016/j.ajhg.2023.03.017},
url = {https://doi.org/10.1016/j.ajhg.2023.03.017}
}RIS
TY - JOUR TI - De novo variants implicate chromatin modification, transcriptional regulation, and retinoic acid signaling in syndromic craniosynostosis. AU - Timberlake AT AU - McGee S AU - Allington G AU - Kiziltug E AU - Wolfe EM AU - Stiegler AL AU - Boggon TJ AU - Sanyoura M AU - Morrow M AU - Wenger TL AU - Fernandes EM AU - Caluseriu O AU - Persing JA AU - Jin SC AU - Lifton RP AU - Kahle KT AU - Kruszka P PY - 2023 JO - American journal of human genetics DO - 10.1016/j.ajhg.2023.03.017 UR - https://doi.org/10.1016/j.ajhg.2023.03.017 ER -
APA
AT, T., S, M., G, A., E, K., EM, W., AL, S., TJ, B., M, S., M, M., TL, W., EM, F., O, C., JA, P., SC, J., RP, L., KT, K., & P, K. (2023). De novo variants implicate chromatin modification, transcriptional regulation, and retinoic acid signaling in syndromic craniosynostosis.. American journal of human genetics. https://doi.org/10.1016/j.ajhg.2023.03.017
Source records
- pubmed · retrieved 2026-09-27T15:09:31.244Z