Souche, E., Beltran, S., & Weiss, M. M. (2022). Recommendations for whole genome sequencing in diagnostics for rare diseases.
Citación estilo ChicagoSouche, Erika, Sergi Beltran, y Marjan M. Weiss. Recommendations for Whole Genome Sequencing in Diagnostics for Rare Diseases. 2022.
Cita MLASouche, Erika, Sergi Beltran, y Marjan M. Weiss. Recommendations for Whole Genome Sequencing in Diagnostics for Rare Diseases. 2022.
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