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Dive into the research topics of 'Familial 22q11.2 deletions in DiGeorge/velocardiofacial syndrome are predominantly smaller than the commonly observed 3Mb'. Together they form a unique fingerprint.- Sort by
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Adewale Adeyinka, Kimberly J. Stockero, Heather C. Flynn, Cindy P. Lorentz, Rhett P. Ketterling, Syed M. Jalal
Research output: Contribution to journal › Article › peer-review