export default function WESInfo() { const points = [ "Whole Exome Sequencing (WES) is recommended for individuals with unexplained genetic disorders, complex or atypical clinical presentations, or when prior genetic tests have been inconclusive.", "It is especially valuable in diagnosing rare inherited diseases, uncovering the cause of developmental delays, intellectual disabilities, or early-onset neurological conditions, and providing insights for personalized treatment planning.", "WES can help identify genetic causes in a wide range of rare disorders." ]; return (

Who Should Consider Whole Exome Sequencing (WES)?

); }