A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2
Johns Hopkins Medicine · Johns Hopkins University · +8 more institutions
Indexed incrossrefpubmed
Abstract
No abstract available for this paper.
Citation impact
1,773
total citations
- FWCI
- 37.73
- Percentile
- 100%
- References
- 27
Citations per year
Authors
24- BLBart LoeysCorresponding
Johns Hopkins Medicine, Johns Hopkins University
- JCJunji Chen
Johns Hopkins University, Howard Hughes Medical Institute, Johns Hopkins Medicine
- ENEnid Neptune
Johns Hopkins Medicine, Johns Hopkins University
- DPDaniel P. Judge
Johns Hopkins Medicine, Johns Hopkins University
- MPMegan Podowski
Johns Hopkins University, Johns Hopkins Medicine
Topics & keywords
Topics
Keywords
- Biology
- Craniofacial
- Craniosynostosis
- Phenotype
- Transforming growth factor beta
- Allele
- Endocrinology
- Genetics
UN Sustainable Development Goals
- Good health and well-being
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