Hong et al., 2016
- Dominant-negative Kinase Domain Mutations in FGFR1 Can Explain the Clinical Severity of Hartsfield Syndrome.
Human molecular genetics
25(10):1912-1922
Full text @ Hum. Mol. Genet.
| Marker Type | Symbol | Name |
|---|---|---|
| Gene | chrd | chordin |
| Gene | dusp6 | dual specificity phosphatase 6 |
| Gene | fgfr1a | fibroblast growth factor receptor 1a |
| Gene | fgfr1b | fibroblast growth factor receptor 1b |
| Gene | hbbe1.1 | hemoglobin beta embryonic-1.1 |