Φορτώνει......
Gain-of-function variants and overexpression of RUNX2 in patients with nonsyndromic midline craniosynostosis
Craniosynostosis (CS), the premature fusion of one or more cranial sutures, is a relatively common congenital anomaly, occurring in 3–5 per 10,000 live births. Nonsyndromic CS (NCS) accounts for up to 80% of all CS cases, yet the genetic factors contributing to the disorder remain largely unknown. T...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Bone |
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| Κύριοι συγγραφείς: | , , , , , , , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
2020
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7358991/ https://ncbi.nlm.nih.gov/pubmed/32360898 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bone.2020.115395 |
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