Autor: M. Cecilia Poli

Decoding complex inherited phenotypes in rare disorders: the DECIPHERD initiative for rare undiagnosed diseases in Chile

Ene 4, 2024

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por

M. Cecilia Poli

en Articulos, EurJHumGen

European Journal of Human Genetics, Published online: 04 January 2024; doi:10.1038/s41431-023-01523-5Decoding complex inherited phenotypes in rare disorders: the DECIPHERD initiative for rare undiagnosed diseases in Chile