Targeted Sequencing of Candidate Regions Associated with Sagittal and Metopic Nonsyndromic Craniosynostosis

Craniosynostosis (CS) is a major birth defect in which one or more skull sutures fuse prematurely. We previously performed a genome-wide association study (GWAS) for sagittal non-syndromic CS (sNCS), identifying associations downstream from BMP2 on 20p12.3 and intronic to BBS9 on 7p14.3; analyses of...

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Detalles Bibliográficos
Autores principales: Justice, Cristina M., Musolf, Anthony M., Cuellar, Araceli, Lattanzi, Wanda, Simeonov, Emil, Kaneva, Radka, Paschall, Justin, Cunningham, Michael, Wilkie, Andrew O. M., Wilson, Alexander F., Romitti, Paul A., Boyadjiev, Simeon A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9141801/
https://www.ncbi.nlm.nih.gov/pubmed/35627201
http://dx.doi.org/10.3390/genes13050816

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9141801/
https://www.ncbi.nlm.nih.gov/pubmed/35627201
http://dx.doi.org/10.3390/genes13050816

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