Genome sequencing with gene panel-based analysis for rare inherited conditions in a publicly funded healthcare system: implications for future testing : implications for future testing
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Hocking , L , Andrews , C , Armstrong , C , Ansari , M , Baty , D , Berg , J , Bradley , T , Clark , C , Diamond , A , Doherty , J , Lampe , A , McGowan , R , Moore , D J , O'Sullivan , D , Purvis , A , Santoyo-Lopez , J , Westwood , P , Abbott , M , Williams , N , Scottish Genomes Partnership , Aitman , T J & Miedzybrodzka , Z 2022 , ' Genome sequencing with gene panel-based analysis for rare inherited conditions in a publicly funded healthcare system: implications for future testing : implications for future testing ' , European Journal of Human Genetics . https://doi.org/10.1038/s41431-022-01226-3
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