Laue et al., 2011
- Craniosynostosis and Multiple Skeletal Anomalies in Humans and Zebrafish Result from a Defect in the Localized Degradation of Retinoic Acid.
American journal of human genetics
89(5):595-606
Full text @ Am. J. Hum. Genet.
| Marker Type | Symbol | Name |
|---|---|---|
| Gene | ankha | ANKH inorganic pyrophosphate transport regulator a |
| Gene | ankhb | ANKH inorganic pyrophosphate transport regulator b |
| Gene | col10a1a | collagen, type X, alpha 1a |
| Gene | col1a1a | collagen, type I, alpha 1a |
| Gene | cyp26b1 | cytochrome P450, family 26, subfamily b, polypeptide 1 |
| Gene | fgf23 | fibroblast growth factor 23 |
| Gene | phex | phosphate regulating endopeptidase homolog, X-linked |
| Gene | sost | sclerostin |
| Gene | sox9a | SRY-box transcription factor 9a |
| Gene | sparc | secreted protein, acidic, cysteine-rich (osteonectin) |
| Gene | spp1 | secreted phosphoprotein 1 |