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PBX-WNT-P63-IRF6 pathway in nonsyndromic cleft lip and palate
Nonsyndromic cleft lip and palate (NSCLP) is one of the most common craniofacial anomalies in humans, affecting more than 135,000 newborns worldwide. NSCLP has a multifactorial etiology with more than 50 genes postulated to play an etiologic role. The genetic pathway comprised of Pbx-Wnt-p63-Irf6 ge...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Birth Defects Res |
|---|---|
| Prif Awduron: | , , , , , , , , , , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
2019
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| Pynciau: | |
| Mynediad Ar-lein: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7325739/ https://ncbi.nlm.nih.gov/pubmed/31825181 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/bdr2.1630 |
| Tagiau: |
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