APA (7th ed.) Citation

K, L., K, T., L, M., A, M., A, B., M, M., . . . F, V. (2025). Research-Based Whole Genome Sequencing Identifies Biallelic Loss of Function Variants in DOCK3 Gene Causing DOCK3-Related Disorder: The End of a Diagnostic Journey for This Family. Clinical genetics, 108(1), 109. https://doi.org/10.1111/cge.14741

Chicago Style (17th ed.) Citation

K, Liaqat, Treat K, Mantcheva L, McLaughlin A, Breman A, McPheron M, Conboy E, and Vetrini F. "Research-Based Whole Genome Sequencing Identifies Biallelic Loss of Function Variants in DOCK3 Gene Causing DOCK3-Related Disorder: The End of a Diagnostic Journey for This Family." Clinical Genetics 108, no. 1 (2025): 109. https://doi.org/10.1111/cge.14741.

MLA (9th ed.) Citation

K, Liaqat, et al. "Research-Based Whole Genome Sequencing Identifies Biallelic Loss of Function Variants in DOCK3 Gene Causing DOCK3-Related Disorder: The End of a Diagnostic Journey for This Family." Clinical Genetics, vol. 108, no. 1, 2025, p. 109, https://doi.org/10.1111/cge.14741.