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From Genotype to Phenotype: Clinical Assessment and Participant Perspective of a Secondary Genomic Finding Associated with Long QT Syndrome
Genomic variants associated with inherited cardiac conditions yet detected incidentally (‘secondary findings’) are likely to arise with increasing frequency as genome sequencing transitions into clinical practice. Since genotyping has until recently been directed by clinical diagnosis, assessment an...
সংরক্ষণ করুন:
| প্রকাশিত: | Circ Genom Precis Med |
|---|---|
| প্রধান লেখক: | , , , , |
| বিন্যাস: | Artigo |
| ভাষা: | Inglês |
| প্রকাশিত: |
2018
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| বিষয়গুলি: | |
| অনলাইন ব্যবহার করুন: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6217934/ https://ncbi.nlm.nih.gov/pubmed/30354302 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCGEN.118.002316 |
| ট্যাগগুলো: |
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