Identification of a novel and a recurrent CDC45 variant in a Chinese family with Meier-Gorlin syndrome 7 and a literature review.
- DOI
- 10.3389/fgene.2026.1893476
- Published
- 2026
- Container
- Frontiers in genetics
- Publisher
- Not recorded
- Open access
- yes
Credibility signals
limited evidence Score 45/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.
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Cite this work
BibTeX
@article{allodium:10.3389/fgene.2026.1893476,
title = {Identification of a novel and a recurrent CDC45 variant in a Chinese family with Meier-Gorlin syndrome 7 and a literature review.},
author = {Zhao Y and Fu Y and Zhang S and Han Y and Zhu J and Liu W and Li S and Xiao D and Liu Y and Wang L and Zhang R and Cheng W and Ren K and Zhang X and Chen M and Abdullah and Kalsoom UE and Bibi N and Khan S and Fan F and Jia T and Lin X and Li W and Li Z and Nishimura G and Yamada T and Cai N and Shukunami C and Tian Z and Chen X and Ikegawa S and Qiang R and Guo L},
year = {2026},
journal = {Frontiers in genetics},
doi = {10.3389/fgene.2026.1893476},
url = {https://doi.org/10.3389/fgene.2026.1893476}
}RIS
TY - JOUR TI - Identification of a novel and a recurrent CDC45 variant in a Chinese family with Meier-Gorlin syndrome 7 and a literature review. AU - Zhao Y AU - Fu Y AU - Zhang S AU - Han Y AU - Zhu J AU - Liu W AU - Li S AU - Xiao D AU - Liu Y AU - Wang L AU - Zhang R AU - Cheng W AU - Ren K AU - Zhang X AU - Chen M AU - Abdullah AU - Kalsoom UE AU - Bibi N AU - Khan S AU - Fan F AU - Jia T AU - Lin X AU - Li W AU - Li Z AU - Nishimura G AU - Yamada T AU - Cai N AU - Shukunami C AU - Tian Z AU - Chen X AU - Ikegawa S AU - Qiang R AU - Guo L PY - 2026 JO - Frontiers in genetics DO - 10.3389/fgene.2026.1893476 UR - https://doi.org/10.3389/fgene.2026.1893476 ER -
APA
Y, Z., Y, F., S, Z., Y, H., J, Z., W, L., S, L., D, X., Y, L., L, W., R, Z., W, C., K, R., X, Z., M, C., Abdullah, UE, K., N, B., S, K., F, F., T, J., X, L., W, L., Z, L., G, N., T, Y., N, C., C, S., Z, T., X, C., S, I., R, Q., & L, G. (2026). Identification of a novel and a recurrent CDC45 variant in a Chinese family with Meier-Gorlin syndrome 7 and a literature review.. Frontiers in genetics. https://doi.org/10.3389/fgene.2026.1893476
Source records
- pubmed · retrieved 2026-09-26T06:47:14.669Z