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Dive into the research topics of 'Prader-Willi phenotype caused by paternal deficiency for the HBII-85 C/D box small nucleolar RNA cluster'. Together they form a unique fingerprint.- Sort by
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Trilochan Sahoo, Daniela Del Gaudio, Jennifer R. German, Marwan Shinawi, Sarika U. Peters, Richard E. Person, Adolfo Garnica, Sau Wai Cheung, Arthur L. Beaudet
Research output: Contribution to journal › Article › peer-review