Molecular Diagnostic Yield of Exome Sequencing in Patients With Congenital Hydrocephalus: A Systematic Review and Meta-Analysis

IMPORTANCE: Exome sequencing (ES) has been established as the preferred first line of diagnostic testing for certain neurodevelopmental disorders, such as global developmental delay and autism spectrum disorder; however, current recommendations are not specific to or inclusive of congenital hydrocep...

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Detalles Bibliográficos
Autores principales: Greenberg, Ana B. W., Mehta, Neel H., Allington, Garrett, Jin, Sheng Chih, Moreno-De-Luca, Andrés, Kahle, Kristopher T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Medical Association 2023
Materias:
Original Investigation
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10665979/
https://www.ncbi.nlm.nih.gov/pubmed/37991765
http://dx.doi.org/10.1001/jamanetworkopen.2023.43384

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10665979/
https://www.ncbi.nlm.nih.gov/pubmed/37991765
http://dx.doi.org/10.1001/jamanetworkopen.2023.43384

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