Journal
JAMA PEDIATRICS
Volume 175, Issue 3, Pages 310-313Publisher
AMER MEDICAL ASSOC
DOI: 10.1001/jamapediatrics.2020.4878
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Funding
- Yale-National Institutes of Health Center for Mendelian Genomics [5U54HG006504, R01 NS111029-01A1, R01 NS109358, K12 228168]
- Rudi Schulte Research Institute
- James Hudson Brown-Alexander Brown Coxe Postdoctoral Fellowship
- American Heart Association Postdoctoral Fellowship
- National Heart, Lung, and Blood Institute of the National Institutes of Health [K99HL143036, R00HL143036-02]
- National Institutes of Health Medical Scientist Training Program Training Grant [T32GM136651]
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This study evaluates the use of whole-exome sequencing as a diagnostic tool in a cohort of neurosurgically treated congenital hydrocephalus patients.
This study evaluates whole-exome sequencing as a diagnostic tool in a cohort of neurosurgically treated congenital hydrocephalus probands.
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