Refinements and considerations for trio whole-genome sequence analysis when investigating Mendelian diseases presenting in early childhood.

MLA

French, Courtney E., et al. “Refinements and Considerations for Trio Whole-Genome Sequence Analysis When Investigating Mendelian Diseases Presenting in Early Childhood.” HGG Advances, vol. 3, no. 3, Apr. 2022, p. 100113. EBSCOhost, https://doi.org/10.1016/j.xhgg.2022.100113.

APA

French, C. E., Dolling, H., Mégy, K., Sanchis-Juan, A., Kumar, A., Delon, I., Wakeling, M., Mallin, L., Agrawal, S., Austin, T., Walston, F., Park, S.-M., Parker, A., Piyasena, C., Bradbury, K., Ellard, S., Rowitch, D. H., & Raymond, F. L. (2022). Refinements and considerations for trio whole-genome sequence analysis when investigating Mendelian diseases presenting in early childhood. HGG Advances, 3(3), 100113. https://doi.org/10.1016/j.xhgg.2022.100113

Chicago

French, Courtney E, Helen Dolling, Karyn Mégy, Alba Sanchis-Juan, Ajay Kumar, Isabelle Delon, Matthew Wakeling, et al. 2022. “Refinements and Considerations for Trio Whole-Genome Sequence Analysis When Investigating Mendelian Diseases Presenting in Early Childhood.” HGG Advances 3 (3): 100113. doi:10.1016/j.xhgg.2022.100113.