A novel de novo variant in the RUNX2 gene causes cleidocranial dysplasia in a Malian girl.
- DOI
- 10.1002/ccr3.8551
- Published
- 2024 Feb
- Container
- Clinical case reports
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1002/ccr3.8551,
title = {A novel de novo variant in the RUNX2 gene causes cleidocranial dysplasia in a Malian girl.},
author = {Cissé L and Yalcouyé A and Touré KO and Coulibaly Y and Maiga AB and Bamba S and Diallo D and Diarra S and Taméga A and Traoré O and Kotioumbé M and Sangaré MA and Ba HO and Simaga A and Koné FI and Samassekou O and Koné A and Guinto CO and Landouré G and H3Africa consortium},
year = {2024},
journal = {Clinical case reports},
doi = {10.1002/ccr3.8551},
url = {https://doi.org/10.1002/ccr3.8551}
}RIS
TY - JOUR TI - A novel de novo variant in the RUNX2 gene causes cleidocranial dysplasia in a Malian girl. AU - Cissé L AU - Yalcouyé A AU - Touré KO AU - Coulibaly Y AU - Maiga AB AU - Bamba S AU - Diallo D AU - Diarra S AU - Taméga A AU - Traoré O AU - Kotioumbé M AU - Sangaré MA AU - Ba HO AU - Simaga A AU - Koné FI AU - Samassekou O AU - Koné A AU - Guinto CO AU - Landouré G AU - H3Africa consortium PY - 2024 JO - Clinical case reports DO - 10.1002/ccr3.8551 UR - https://doi.org/10.1002/ccr3.8551 ER -
APA
L, C., A, Y., KO, T., Y, C., AB, M., S, B., D, D., S, D., A, T., O, T., M, K., MA, S., HO, B., A, S., FI, K., O, S., A, K., CO, G., G, L., & consortium, H. (2024). A novel de novo variant in the RUNX2 gene causes cleidocranial dysplasia in a Malian girl.. Clinical case reports. https://doi.org/10.1002/ccr3.8551
Source records
- pubmed · retrieved 2026-09-26T13:44:12.333Z