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Dive into the research topics of 'Missense mutations in FBN1 exons 41 and 42 cause Weill-Marchesani syndrome with thoracic aortic disease and Marfan syndrome'. Together they form a unique fingerprint.- Sort by
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Alana Cecchi, Naomi Ogawa, Hugo R. Martinez, Alicia Carlson, Yuxin Fan, Daniel J. Penny, Dong Chuan Guo, Steven Eisenberg, Hazim Safi, Anthony Estrera, Richard A. Lewis, Deborah Meyers, Dianna M. Milewicz
Research output: Contribution to journal › Article › peer-review