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Dive into the research topics of 'Persistent lung disease in adults with NKX2.1 mutation and familial neuroendocrine cell hyperplasia of infancy'. Together they form a unique fingerprint.- Sort by
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Rebekah J. Nevel, Errine T. Garnett, John A. Worrell, Ronald L. Morton, Lawrence M. Nogee, Timothy S. Blackwell, Lisa R. Young
Research output: Contribution to journal › Article › peer-review