Cecchi, A. C., Vengoechea, E. S., Kaseniit, K. E., Hardy, M. W., Kiger, L. A., Mehta, N., . . . Grinzaid, K. A. (2019). Screening for Tay‐Sachs disease carriers by full‐exon sequencing with novel variant interpretation outperforms enzyme testing in a pan‐ethnic cohort. Mol Genet Genomic Med.
Citación estilo ChicagoCecchi, Alana C., et al. "Screening for Tay‐Sachs Disease Carriers By Full‐exon Sequencing With Novel Variant Interpretation Outperforms Enzyme Testing in a Pan‐ethnic Cohort." Mol Genet Genomic Med 2019.
Cita MLACecchi, Alana C., et al. "Screening for Tay‐Sachs Disease Carriers By Full‐exon Sequencing With Novel Variant Interpretation Outperforms Enzyme Testing in a Pan‐ethnic Cohort." Mol Genet Genomic Med 2019.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.