A homozygous variant in the Lamin B receptor gene LBR results in a non-lethal skeletal dysplasia without Pelger-Huët anomaly.

MLA

Collins, Meagan, et al. “A Homozygous Variant in the Lamin B Receptor Gene LBR Results in a Non-Lethal Skeletal Dysplasia without Pelger-Huët Anomaly.” Bone, vol. 141, Dec. 2020, p. 115601. EBSCOhost, https://doi.org/10.1016/j.bone.2020.115601.

APA

Collins, M., Miranda, V., Rousseau, J., Kratz, L. E., & Campeau, P. M. (2020). A homozygous variant in the Lamin B receptor gene LBR results in a non-lethal skeletal dysplasia without Pelger-Huët anomaly. Bone, 141, 115601. https://doi.org/10.1016/j.bone.2020.115601

Chicago

Collins, Meagan, Valancy Miranda, Justine Rousseau, Lisa E Kratz, and Philippe M Campeau. 2020. “A Homozygous Variant in the Lamin B Receptor Gene LBR Results in a Non-Lethal Skeletal Dysplasia without Pelger-Huët Anomaly.” Bone 141 (December): 115601. doi:10.1016/j.bone.2020.115601.