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A comprehensive screen of genes implicated in craniosynostosis.
Recent advances in human molecular genetics have identified mutations in the TWIST, FGFR-1, FGFR-2 and FGFR-3 genes to be important causes of craniosynostosis. Despite this, however, mutations cannot be identified in the majority of patients. This study reports the first comprehensive screen of muta...
Tallennettuna:
| Päätekijä: | |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2003
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1964413/ https://ncbi.nlm.nih.gov/pubmed/14629875 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1308/003588403322520708 |
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