APA (7th ed.) Citation

Uwibambe, E., Yalcouyé, A., Aboagye, E. T., Xhakaza, L., Popel, K., Dukuze, N., . . . Wonkam, A. (2025). Exome sequencing revealed a novel homozygous variant in TRMT61 A in a multiplex family with atypical Cornelia de Lange Syndrome from Rwanda. BMC Medical Genomics, 18(1), 1. https://doi.org/10.1186/s12920-025-02153-0

Chicago Style (17th ed.) Citation

Uwibambe, Esther, et al. "Exome Sequencing Revealed a Novel Homozygous Variant in TRMT61 A in a Multiplex Family with Atypical Cornelia De Lange Syndrome from Rwanda." BMC Medical Genomics 18, no. 1 (2025): 1. https://doi.org/10.1186/s12920-025-02153-0.

MLA (9th ed.) Citation

Uwibambe, Esther, et al. "Exome Sequencing Revealed a Novel Homozygous Variant in TRMT61 A in a Multiplex Family with Atypical Cornelia De Lange Syndrome from Rwanda." BMC Medical Genomics, vol. 18, no. 1, 2025, p. 1, https://doi.org/10.1186/s12920-025-02153-0.