Trait − driven analysis of the 2p15p16.1 microdeletion syndrome suggests a complex pattern of interactions between candidate genes

BACKGROUND: Individuals with the 2p15p16.1 microdeletion syndrome share a complex phenotype including neurodevelopmental delay, brain malformations, microcephaly, and autistic behavior. The analysis of the shortest region of overlap (SRO) between deletions in ~ 40 patients has led to the identificat...

Descripción completa

Detalles Bibliográficos
Autores principales: Miceli, Martina, Failla, Pinella, Saccuzzo, Lucia, Galesi, Ornella, Amata, Silvestra, Romano, Corrado, Bonaglia, Maria Clara, Fichera, Marco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Nature Singapore 2023
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10027778/
https://www.ncbi.nlm.nih.gov/pubmed/36807877
http://dx.doi.org/10.1007/s13258-023-01369-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10027778/
https://www.ncbi.nlm.nih.gov/pubmed/36807877
http://dx.doi.org/10.1007/s13258-023-01369-7

Ejemplares similares