Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5718908 | The Journal of Pediatrics | 2017 | 6 Pages |
Abstract
We present cases of 3 children diagnosed with the same genetic condition, Gitelman syndrome, at different stages using various genetic methods: panel testing, targeted single gene sequencing, and exome sequencing. We discuss the advantages and disadvantages of each method and review the potential of genomic sequencing for early disease detection.
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Authors
Hengameh MD, PhD, Teresa N. MD, Ben MD, Adnan MD, Joseph T.C. MD, PhD,