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Dive into the research topics of 'Familial Exudative Vitreoretinopathy–Like Phenotype in a Patient With Microcephaly and TUBGCP6 Mutations'. Together they form a unique fingerprint.- Sort by
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Jesse D. Sengillo, Noy Ashkenazy, Marissa K. Shoji, Prashanth Iyer, Hailey K. Robles-Holmes, Ashley Lopez, Nicolas A. Yannuzzi, Catherin I. Negron, Audina M. Berrocal
Research output: Contribution to journal › Article › peer-review