Scaling genomic reanalysis to unlock diagnoses and transform rare disease care.
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Nonadherence to guidelines for genetic testing in families with ovarian cancer shows racial bias.
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Preferences of parents from diverse backgrounds on genomic screening of apparently healthy newborns.
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Vitelline vascular remnant causing intestinal obstruction in a patient with TARP syndrome.
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Delayed diagnosis and racial bias in children with genetic conditions.
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Lysinuric protein intolerance: Pearls to detect this otherwise easily missed diagnosis.
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Shortage of generic neurologic therapeutics: An escalating threat to patient care.
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Inpatient cost analysis for treatment of myasthenia gravis.
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