Should secondary pharmacogenomic variants be actively screened and reported when diagnostic genome-wide sequencing is performed in a child?

Author:

Friedman Jan M.ORCID,Bombard Yvonne,Carleton Bruce,Issa Amalia M.,Knoppers Bartha,Plon Sharon E.,Rahimzadeh Vasiliki,Relling Mary V.,Williams Marc S.,van Karnebeek Clara,Vears Danya,Cornel Martina C.

Publisher

Elsevier BV

Subject

Genetics (clinical)

Reference129 articles.

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