APA (7th ed.) Citation

L, P., V, P., A, C., A, B., C, B. d. R., A, C., . . . D, V. (2023). Contribution of whole genome sequencing in the molecular diagnosis of mosaic partial deletion of the NF1 gene in neurofibromatosis type 1. Human genetics, 142(1), 1. https://doi.org/10.1007/s00439-022-02476-3

Chicago Style (17th ed.) Citation

L, Pacot, et al. "Contribution of Whole Genome Sequencing in the Molecular Diagnosis of Mosaic Partial Deletion of the NF1 Gene in Neurofibromatosis Type 1." Human Genetics 142, no. 1 (2023): 1. https://doi.org/10.1007/s00439-022-02476-3.

MLA (9th ed.) Citation

L, Pacot, et al. "Contribution of Whole Genome Sequencing in the Molecular Diagnosis of Mosaic Partial Deletion of the NF1 Gene in Neurofibromatosis Type 1." Human Genetics, vol. 142, no. 1, 2023, p. 1, https://doi.org/10.1007/s00439-022-02476-3.