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Dive into the research topics of 'Severe Cleidocranial dysplasia and hypophosphatasia in a child with microdeletion of the C-terminal region of RUNX2'. Together they form a unique fingerprint.- Sort by
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Areeg H. El-Gharbawy, Joseph N. Peeden, Ralph S. Lachman, John M. Graham, Stephen R. Moore, David L. Rimoin
Research output: Contribution to journal › Article › peer-review