Cargando…
Evidence for contribution of common genetic variants within chromosome 8p21.2-8p21.1 to restricted and repetitive behaviors in autism spectrum disorders
BACKGROUND: Restricted and Repetitive Behaviors (RRB), one of the core symptom categories for Autism Spectrum Disorders (ASD), comprises heterogeneous groups of behaviors. Previous research indicates that there are two or more factors (subcategories) within the RRB domain. In an effort to identify c...
Autores principales: | Tao, Yu, Gao, Hui, Ackerman, Benjamin, Guo, Wei, Saffen, David, Shugart, Yin Yao |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4774106/ https://www.ncbi.nlm.nih.gov/pubmed/26931105 http://dx.doi.org/10.1186/s12864-016-2475-y |
Ejemplares similares
-
Autism and severe clinical phenotype in a patient with 8p21.2p11.21 deletion: Case report and literature review
por: Arghir, Aurora, et al.
Publicado: (2020) -
Ehlers-Danlos Syndrome, Hypermobility Type, Is Linked to Chromosome 8p22-8p21.1 in an Extended Belgian Family
por: Syx, Delfien, et al.
Publicado: (2015) -
Novel 12 Mb interstitial deletion of chromosome 8p11.22-p21.2: a case report
por: Dai, Jincheng, et al.
Publicado: (2022) -
Prenatal Diagnosis and Genetic Analysis of 21q21.1–q21.2 Aberrations in Seven Chinese Pedigrees
por: Hu, Huamei, et al.
Publicado: (2021) -
A prenatal diagnosis case of partial duplication 21q21.1-q21.2 with normal phenotype maternally inherited
por: Jin, Chunyan, et al.
Publicado: (2021)