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Dive into the research topics of 'Xp22.3 microdeletion syndrome with microphthalmia, sclerocornea, linear skin defects, and congenital heart defects'. Together they form a unique fingerprint.- Sort by
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N. M. Lindor, V. V. Michels, D. A. Hoppe, D. J. Driscoll, J. A. Leavitt, G. W. Dewald
Research output: Contribution to journal › Article › peer-review