Results from Genetic Studies in Patients Affected with Craniosynostosis: Clinical and Molecular Aspects

Background: Craniosynostosis (CS) represents a highly heterogeneous genetic condition whose genetic background has not been yet revealed. The abnormality occurs either in isolated form or syndromic, as an element of hundreds of different inborn syndromes. Consequently, CS may often represent a chall...

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Detalles Bibliográficos
Autores principales: Bukowska-Olech, Ewelina, Sowińska-Seidler, Anna, Larysz, Dawid, Gawliński, Paweł, Koczyk, Grzegorz, Popiel, Delfina, Gurba-Bryśkiewicz, Lidia, Materna-Kiryluk, Anna, Adamek, Zuzanna, Szczepankiewicz, Aleksandra, Dominiak, Paweł, Glista, Filip, Matuszewska, Karolina, Jamsheer, Aleksander
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Molecular Biosciences
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9112228/
https://www.ncbi.nlm.nih.gov/pubmed/35591945
http://dx.doi.org/10.3389/fmolb.2022.865494

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9112228/
https://www.ncbi.nlm.nih.gov/pubmed/35591945
http://dx.doi.org/10.3389/fmolb.2022.865494

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