Cadieux-Dion, M., Safina, N. P., Engleman, K., Saunders, C., Repnikova, E., Raje, N., . . . Thiffault, I. (2018). Novel heterozygous pathogenic variants in CHUK in a patient with AEC-like phenotype, immune deficiencies and 1q21.1 microdeletion syndrome: A case report. BMC Med Genet.
Citação norma ChicagoCadieux-Dion, Maxime, et al. "Novel Heterozygous Pathogenic Variants in CHUK in a Patient With AEC-like Phenotype, Immune Deficiencies and 1q21.1 Microdeletion Syndrome: A Case Report." BMC Med Genet 2018.
Deismireacht MLACadieux-Dion, Maxime, et al. "Novel Heterozygous Pathogenic Variants in CHUK in a Patient With AEC-like Phenotype, Immune Deficiencies and 1q21.1 Microdeletion Syndrome: A Case Report." BMC Med Genet 2018.
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