APA (7th ed.) Citation

C, v. d. L., K, T., TE, P., ØL, H., ØL, B., KB, B., . . . WM, T. (2022). Heterozygous variants in ZBTB7A cause a neurodevelopmental disorder associated with symptomatic overgrowth of pharyngeal lymphoid tissue, macrocephaly, and elevated fetal hemoglobin. American journal of medical genetics. Part A, 188(1), 272. https://doi.org/10.1002/ajmg.a.62492

Chicago Style (17th ed.) Citation

C, von der Lippe, et al. "Heterozygous Variants in ZBTB7A Cause a Neurodevelopmental Disorder Associated with Symptomatic Overgrowth of Pharyngeal Lymphoid Tissue, Macrocephaly, and Elevated Fetal Hemoglobin." American Journal of Medical Genetics. Part A 188, no. 1 (2022): 272. https://doi.org/10.1002/ajmg.a.62492.

MLA (9th ed.) Citation

C, von der Lippe, et al. "Heterozygous Variants in ZBTB7A Cause a Neurodevelopmental Disorder Associated with Symptomatic Overgrowth of Pharyngeal Lymphoid Tissue, Macrocephaly, and Elevated Fetal Hemoglobin." American Journal of Medical Genetics. Part A, vol. 188, no. 1, 2022, p. 272, https://doi.org/10.1002/ajmg.a.62492.