Swetha Narayanan

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Publications (3)

• GABRG1 variant as a potential novel cause of epileptic encephalopathy, hypotonia, and global developmental delay.
  American journal of medical genetics. Part A 2022 DOI: 10.1002/ajmg.a.62969
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• Exploring the Issues Surrounding Clinical Exome Sequencing in the Prenatal Setting.
  Journal of genetic counseling 2018 DOI: 10.1007/s10897-018-0245-5
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• Use of Exome Sequencing for Infants in Intensive Care Units: Ascertainment of Severe Single-Gene Disorders and Effect on Medical Management.
  JAMA pediatrics 2017 DOI: 10.1001/jamapediatrics.2017.3438
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