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Dive into the research topics of 'Fanconi anemia-like presentation in an infant with constitutional deletion of 21q including the RUNX1 gene'. Together they form a unique fingerprint.- Sort by
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Eleanor S. Click, Barbara Cox, Susan B. Olson, Markus Grompe, Yassmine Akkari, Lisa A. Moreau, Akiko Shimamura, Darci L. Sternen, Yajuan J. Liu, Kathleen A. Leppig, Dana C. Matthews, Melissa A. Parisi
Research output: Contribution to journal › Article › peer-review