{"id":5290,"date":"2022-09-21T15:08:47","date_gmt":"2022-09-21T13:08:47","guid":{"rendered":"https:\/\/www.hartwigmedicalfoundation.nl\/?post_type=quoutes&#038;p=5290"},"modified":"2023-04-14T15:17:26","modified_gmt":"2023-04-14T13:17:26","slug":"gdf","status":"publish","type":"quoutes","link":"https:\/\/www.hartwigmedicalfoundation.nl\/en\/quoutes\/gdf\/","title":{"rendered":"Jos\u00e9 van den Berg"},"content":{"rendered":"\n<p class=\"wp-block-paragraph\">By using WGS, we took a step forward in molecular diagnostics in our department from the analysis of less than 100 genes to approximately 20,000 genes per patient. 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