APA (7th ed.) Citation

Tisserant, E., Vitobello, A., Callegarin, D., Verdez, S., Bruel, A., Aho Glele, L. S., . . . Payet, M. (2022). Copy number variants calling from WES data through eXome hidden Markov model (XHMM) identifies additional 2.5% pathogenic genomic imbalances smaller than 30 kb undetected by array‐CGH. Annals of Human Genetics, 86(4), 171. https://doi.org/10.1111/ahg.12459

Chicago Style (17th ed.) Citation

Tisserant, Emilie, et al. "Copy Number Variants Calling from WES Data Through EXome Hidden Markov Model (XHMM) Identifies Additional 2.5% Pathogenic Genomic Imbalances Smaller than 30 kb Undetected by Array‐CGH." Annals of Human Genetics 86, no. 4 (2022): 171. https://doi.org/10.1111/ahg.12459.

MLA (9th ed.) Citation

Tisserant, Emilie, et al. "Copy Number Variants Calling from WES Data Through EXome Hidden Markov Model (XHMM) Identifies Additional 2.5% Pathogenic Genomic Imbalances Smaller than 30 kb Undetected by Array‐CGH." Annals of Human Genetics, vol. 86, no. 4, 2022, p. 171, https://doi.org/10.1111/ahg.12459.