Should next-generation sequencing be considered as a first-line genetic investigation for children with early developmental impairment?

Autor: Sarantis F; East and North Hertfordshire NHS Trust, Stevenage, UK frederica.sarantis@nhs.net., Guobadia AO; Paediatrics, East Suffolk and North Essex NHS Foundation Trust, Colchester, UK., Bebars MA; Princess Alexandra Hospital NHS Trust, Harlow, UK., Varma R; Norfolk and Norwich University Hospital NHS Trust, Norwich, UK., Holland JAA; Department of Clinical Neurosciences, University of Cambridge, Cambridge, Cambridgeshire, UK., Ratnaike T; Paediatrics, East Suffolk and North Essex NHS Foundation Trust, Colchester, UK.; Paediatrics, University of Cambridge, Cambridge, UK.

Publikováno v: Archives of disease in childhood [Arch Dis Child] 2024 Oct 29. Date of Electronic Publication: 2024 Oct 29.