Frisk, S., Wachtmeister, A., Laurell, T., Lindstrand, A., Jäntti, N., Malmgren, H., . . . Nordgren, A. (2022). Detection of germline mosaicism in fathers of children with intellectual disability syndromes caused by de novo variants. Molecular Genetics & Genomic Medicine, 10(4), 1. https://doi.org/10.1002/mgg3.1880
Chicago Style (17th ed.) CitationFrisk, Sofia, et al. "Detection of Germline Mosaicism in Fathers of Children with Intellectual Disability Syndromes Caused by De Novo Variants." Molecular Genetics & Genomic Medicine 10, no. 4 (2022): 1. https://doi.org/10.1002/mgg3.1880.
MLA (9th ed.) CitationFrisk, Sofia, et al. "Detection of Germline Mosaicism in Fathers of Children with Intellectual Disability Syndromes Caused by De Novo Variants." Molecular Genetics & Genomic Medicine, vol. 10, no. 4, 2022, p. 1, https://doi.org/10.1002/mgg3.1880.