4.4 Letter

Exome Sequencing as a Potential Diagnostic Adjunct in Sporadic Congenital Hydrocephalus

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JAMA PEDIATRICS
卷 175, 期 3, 页码 310-313

出版社

AMER MEDICAL ASSOC
DOI: 10.1001/jamapediatrics.2020.4878

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资金

  1. Yale-National Institutes of Health Center for Mendelian Genomics [5U54HG006504, R01 NS111029-01A1, R01 NS109358, K12 228168]
  2. Rudi Schulte Research Institute
  3. James Hudson Brown-Alexander Brown Coxe Postdoctoral Fellowship
  4. American Heart Association Postdoctoral Fellowship
  5. National Heart, Lung, and Blood Institute of the National Institutes of Health [K99HL143036, R00HL143036-02]
  6. National Institutes of Health Medical Scientist Training Program Training Grant [T32GM136651]

向作者/读者索取更多资源

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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