Cargando…
A Genome Model to Explain Major Features of Neurodevelopmental Disorders in Newborns
The purpose of this study was to test the hypothesis that infections are linked to chromosomal anomalies that cause neurodevelopmental disorders. In children with disorders in the development of their nervous systems, chromosome anomalies known to cause these disorders were compared with foreign DNA...
Autor principal: | Friedenson, Bernard |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6669855/ https://www.ncbi.nlm.nih.gov/pubmed/31391780 http://dx.doi.org/10.1177/1178222619863369 |
Ejemplares similares
-
The BRCA1/2 pathway prevents hematologic cancers in addition to breast and ovarian cancers
por: Friedenson, Bernard
Publicado: (2007) -
Comment on ‘The incidence of leukaemia in women with BRCA1 and BRCA2 mutations: an International Prospective Cohort Study'
por: Friedenson, Bernard
Publicado: (2016) -
A molecular model for neurodevelopmental disorders
por: Gigek, C O, et al.
Publicado: (2015) -
PACS1-Neurodevelopmental disorder: clinical features and trial readiness
por: Van Nuland, Abigail, et al.
Publicado: (2021) -
Newborn screening for neurodevelopmental diseases: Are we there yet?
por: Chung, Wendy K., et al.
Publicado: (2022)