Labrijn-Marks, I., Somers-Bolman, G. M., In ’t Groen, S. L. M., Hoogeveen-Westerveld, M., Kroos, M. A., Ala-Mello, S., . . . Halley, D. J. (2020). Segmental and total uniparental isodisomy (UPiD) as a disease mechanism in autosomal recessive lysosomal disorders: Evidence from SNP arrays.
Citação norma ChicagoLabrijn-Marks, Ineke, et al. Segmental and Total Uniparental Isodisomy (UPiD) as a Disease Mechanism in Autosomal Recessive Lysosomal Disorders: Evidence from SNP Arrays. 2020.
Citação norma MLALabrijn-Marks, Ineke, et al. Segmental and Total Uniparental Isodisomy (UPiD) as a Disease Mechanism in Autosomal Recessive Lysosomal Disorders: Evidence from SNP Arrays. 2020.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.