Congenital Heart Defects and Skeletal Malformations Syndrome (CHDSKM) Associated with the ABL1 Gene in a Peruvian patient: Case Report.
- DOI
- 10.1177/11795468251406974
- Published
- 2025
- Container
- Clinical Medicine Insights. Cardiology
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1177/11795468251406974,
title = {Congenital Heart Defects and Skeletal Malformations Syndrome (CHDSKM) Associated with the ABL1 Gene in a Peruvian patient: Case Report.},
author = {Arauco-Lázaro D and Purizaca-Rosillo ND and Rojas-Huillca MA and Vásquez-Villanueva S and Gutierrez EL},
year = {2025},
journal = {Clinical Medicine Insights. Cardiology},
doi = {10.1177/11795468251406974},
url = {https://doi.org/10.1177/11795468251406974}
}RIS
TY - JOUR TI - Congenital Heart Defects and Skeletal Malformations Syndrome (CHDSKM) Associated with the ABL1 Gene in a Peruvian patient: Case Report. AU - Arauco-Lázaro D AU - Purizaca-Rosillo ND AU - Rojas-Huillca MA AU - Vásquez-Villanueva S AU - Gutierrez EL PY - 2025 JO - Clinical Medicine Insights. Cardiology DO - 10.1177/11795468251406974 UR - https://doi.org/10.1177/11795468251406974 ER -
APA
D, A., ND, P., MA, R., S, V., & EL, G. (2025). Congenital Heart Defects and Skeletal Malformations Syndrome (CHDSKM) Associated with the ABL1 Gene in a Peruvian patient: Case Report.. Clinical Medicine Insights. Cardiology. https://doi.org/10.1177/11795468251406974
Source records
- pubmed · retrieved 2026-09-26T22:42:54.078Z