HR
Haynes Robinson
Credentials: ·
Research
CRTAP and LEPRE1 mutations in recessive osteogenesis imperfecta
Human Mutation · 2008 · 173 citations
Bent bone dysplasia-FGFR2 type, a distinct skeletal disorder, has deficient canonical FGF signaling
The American Journal of Human Genetics · 2012 · 71 citations
Case report · American Journal of Medical Genetics Part A · 2014 · 65 citations
- BS
8 papers
- DA
6 papers
5 papers
2 papers
2 papers
2 papers
1 paper
1 paper
