APA (7th ed.) Citation

Bukowska-Olech, E., Sowińska-Seidler, A., Wierzba, J., & Jamsheer, A. (2022). SHFLD3 phenotypes caused by 17p13.3 triplication/ duplication encompassing Fingerin (BHLHA9) invariably. Orphanet Journal of Rare Diseases, 17(1), 1. https://doi.org/10.1186/s13023-022-02480-w

Chicago Style (17th ed.) Citation

Bukowska-Olech, Ewelina, Anna Sowińska-Seidler, Jolanta Wierzba, and Aleksander Jamsheer. "SHFLD3 Phenotypes Caused by 17p13.3 Triplication/ Duplication Encompassing Fingerin (BHLHA9) Invariably." Orphanet Journal of Rare Diseases 17, no. 1 (2022): 1. https://doi.org/10.1186/s13023-022-02480-w.

MLA (9th ed.) Citation

Bukowska-Olech, Ewelina, et al. "SHFLD3 Phenotypes Caused by 17p13.3 Triplication/ Duplication Encompassing Fingerin (BHLHA9) Invariably." Orphanet Journal of Rare Diseases, vol. 17, no. 1, 2022, p. 1, https://doi.org/10.1186/s13023-022-02480-w.