TY - JOUR AU - Loeys, B L; Chen, J; Neptune, E R TI - A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2 JO - Nat Genet VL - 37 PY - 2005 DO - 10.1038/ng1511 L3 - PubMed-ID: 15731757 SP - 275 EP - 281 N1 - et al. ER -