A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2

Bart L. Loeys, Junji Chen, Enid R. Neptune, Daniel P. Judge, Megan Podowski, Tammy Holm, Jennifer Meyers, Carmen C. Leitch, Nicholas Katsanis, Neda Sharifi, F. Lauren Xu, Loretha A. Myers, Philip J. Spevak, Duke E. Cameron, Julie De Backer, Jan Hellemans, Yan Chen, Elaine C. Davis, Catherine L. Webb, Wolfram KressPaul Coucke, Daniel B. Rifkin, Anne M. De Paepe, Harry C. Dietz

Research output: Contribution to journal › Article › peer-review

1171 Scopus citations

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Medicine & Life Sciences