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Syndromic craniosynostosis associated with microdeletion of chromosome 19p13.12–19p13.2
Craniosynostosis, a condition in which the cranial sutures prematurely fuse, can lead to elevated intracranial pressure and craniofacial abnormalities in young children. Currently surgical intervention is the only therapeutic option for patients with this condition. Craniosynostosis has been associa...
Tallennettuna:
| Julkaisussa: | Genes Dis |
|---|---|
| Päätekijät: | , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Chongqing Medical University
2015
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4782977/ https://ncbi.nlm.nih.gov/pubmed/26966713 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.gendis.2015.09.001 |
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