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Common skeletal features in rare diseases: New links between ciliopathies and FGF-related syndromes
Congenital skeletal anomalies are rare disorders, with a subset affecting both the cranial and appendicular skeleton. Two categories, craniosynostosis syndromes and chondrodysplasias, frequently result from aberrant regulation of the fibroblast growth factor (FGF) signaling pathway. Our recent work...
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| Main Authors: | , |
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| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Landes Bioscience
2013
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3932950/ https://ncbi.nlm.nih.gov/pubmed/25003013 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/rdis.27109 |
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