Cargando…
Comparative mapping of the 22q11.2 deletion region and the potential of simple model organisms
BACKGROUND: 22q11.2 deletion syndrome (22q11.2DS) is the most common micro-deletion syndrome. The associated 22q11.2 deletion conveys the strongest known molecular risk for schizophrenia. Neurodevelopmental phenotypes, including intellectual disability, are also prominent though variable in severity...
Autores principales: | Guna, Alina, Butcher, Nancy J., Bassett, Anne S. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4487986/ https://www.ncbi.nlm.nih.gov/pubmed/26137170 http://dx.doi.org/10.1186/s11689-015-9113-x |
Ejemplares similares
-
Obesity in adults with 22q11.2 deletion syndrome
por: Voll, S, et al.
Publicado: (2016) -
Adult Height, 22q11.2 Deletion Extent, and Short Stature in 22q11.2 Deletion Syndrome
por: Heung, Tracy, et al.
Publicado: (2022) -
22q11.2 Deletion Syndrome–Associated Parkinson's Disease
por: Boot, Erik, et al.
Publicado: (2018) -
MicroRNA Dysregulation, Gene Networks, and Risk for Schizophrenia in 22q11.2 Deletion Syndrome
por: Merico, Daniele, et al.
Publicado: (2014) -
F72. NEUROCOGNITION AND ADAPTIVE FUNCTIONING IN THE 22Q11.2 DELETION SYNDROME MODEL OF SCHIZOPHRENIA
por: Ania, Fiksinski, et al.
Publicado: (2018)