{"id":"W2114232003","doi":"10.1038/ng1511","title":"A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2","year":2005,"lang":"en","type":"article","venue":"Nature Genetics","topic":"Connective tissue disorders research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":1778,"is_retracted":false,"has_abstract":false,"ca_institutions":"McGill University","funders":"","keywords":"Biology; Craniofacial; Craniosynostosis; Phenotype; Transforming growth factor beta; Allele; Endocrinology; Genetics; Transforming growth factor; Internal medicine; Gene; Medicine","routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false,"invisible_to_affiliation_only":false},"retraction":null,"screen":null}