Epigenomic signature of major congenital heart defects in newborns with Down syndrome

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BACKGROUND: Congenital heart defects (CHDs) affect approximately half of individuals with Down syndrome (DS), but the molecular reasons for incomplete penetrance are unknown. Previous studies have largely focused on identifying genetic risk factors associated with CHDs in individuals with DS, but co...

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Detalles Bibliográficos
Autores principales: Mouat, Julia S., Li, Shaobo, Myint, Swe Swe, Laufer, Benjamin I., Lupo, Philip J., Schraw, Jeremy M., Woodhouse, John P., de Smith, Adam J., LaSalle, Janine M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10559462/
https://www.ncbi.nlm.nih.gov/pubmed/37803336
http://dx.doi.org/10.1186/s40246-023-00540-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10559462/
https://www.ncbi.nlm.nih.gov/pubmed/37803336
http://dx.doi.org/10.1186/s40246-023-00540-1

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