Human Genome Epidemiology Literature Finder
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Query Trace: Abnormalities and CC2D2A[original query] |
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Clinical and Molecular Diagnosis of Joubert Syndrome and Related Disorders. Pediatric neurology 2020 3 106 43-49. Radha Rama Devi Akella, Naushad Shaik Mohammad, Lingappa Loke |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 16, 2024
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