A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2
Bart Loeys(Johns Hopkins Medicine), Junji Chen(Johns Hopkins University), Enid Neptune(Johns Hopkins Medicine), Daniel P. Judge(Johns Hopkins Medicine), Megan Podowski(Johns Hopkins University), Tammy M. Holm(Johns Hopkins Medicine), Jennifer Meyers(Howard Hughes Medical Institute), Carmen C. Leitch(Johns Hopkins University), Nicholas Katsanis(Johns Hopkins University), Neda Sharifi(Johns Hopkins University), Feifei Xu(Johns Hopkins University), Loretha Myers(Johns Hopkins University), Philip J. Spevak(Johns Hopkins University), Duke E. Cameron(Johns Hopkins University), Julie De Backer(Ghent University Hospital), Jan Hellemans(Ghent University Hospital), Yan Chen(New York University), Elaine C. Davis(McGill University), Catherine L. Webb(Northwestern University), Wolfram Kreß(University of Würzburg), Paul Coucke(Ghent University Hospital), Daniel B. Rifkin(New York University), Anne M. De Paepe(Ghent University Hospital), Harry C. Dietz(Howard Hughes Medical Institute)
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