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The Future of Newborn Genomic Testing

Genome sequencing (GS) provides exciting opportunities to rapidly identify a diagnosis in critically ill newborns and children with rare genetic conditions. Nevertheless, there are reasons to remain cautious about the use of GS. Studies to date have been mostly in highly selected populations of babi...

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Detalles Bibliográficos
Autor principal:	Lantos, John D.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2023
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10378699/ https://www.ncbi.nlm.nih.gov/pubmed/37508635 http://dx.doi.org/10.3390/children10071140

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