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Mutation Screening of Candidate Genes in Patients with Nonsyndromic Sagittal Craniosynostosis

BACKGROUND: Craniosynostosis is a condition that includes the premature fusion of one or multiple cranial sutures. Among various craniosynostosis forms, midline sagittal nonsyndromic craniosynostosis (sNSC) is the most prevalent. Although different gene mutations have been identified in some cranios...

Täydet tiedot

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Bibliografiset tiedot
Julkaisussa:Plast Reconstr Surg
Päätekijät: Ye, Xiaoqian, Guilmatre, Audrey, Reva, Boris, Peter, Inga, Heuzé, Yann, Richtsmeier, Joan T., Fox, Deborah J., Goedken, Rhinda J., Jabs, Ethylin W, Romitti, Paul A.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2016
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC4770826/
https://ncbi.nlm.nih.gov/pubmed/26910679
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/01.prs.0000479978.75545.ee
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