Share
Other content recommended for you
- Genomic intensive care: should we perform genome testing in critically ill newborns?
- Parents perspectives on whole genome sequencing for their children: qualified enthusiasm?
- Genomic testing for children with interstitial and diffuse lung disease (chILD): parent satisfaction, understanding and health-related quality of life
- Cancer patients’ views and understanding of genome sequencing: a qualitative study
- Genomics for paediatricians: promises and pitfalls
- Two-step offer and return of multiple types of additional genomic findings to families after ultrarapid trio genomic testing in the acute care setting: a study protocol
- The 100 000 Genomes Project: bringing whole genome sequencing to the NHS
- Comprehensive evaluation of a prospective Australian patient cohort with suspected genetic kidney disease undergoing clinical genomic testing: a study protocol
- Case for genome sequencing in infants and children with rare, undiagnosed or genetic diseases
- Delivering genome sequencing in clinical practice: an interview study with healthcare professionals involved in the 100 000 Genomes Project