2 documents found, page 1 of 1

Sort by Issue Date
go first page go previous page
go to page: 1
go next page go last page
rss feed search results

Recurrent duplications of the annexin A1 gene (ANXA1) in autism spectrum disorders

Correia, CT; Conceição, IC; Oliveira, B; Coelho, J; Sousa, I; Sequeira, AF; Almeida, J; Café, C; Duque, F; Mouga, S; Roberts, W; Gao, K; Lowe, JK

BACKGROUND: Validating the potential pathogenicity of copy number variants (CNVs) identified in genome-wide studies of autism spectrum disorders (ASD) requires detailed assessment of case/control frequencies, inheritance patterns, clinical correlations, and functional impact. Here, we characterize a small recurrent duplication in the annexin A1 (ANXA1) gene, identified by the Autism Genome Project (AGP) study. ...

Date: 2014   |   Origin: Repositório do Centro Hospitalar e Universitário de Coimbra
More info.

Functional characterization of heteromeric human phenylalanine hydroxylase prot...

Sequeira, AF; Leandro, J; Tavares de Almeida, I; Leandro, P

FCT (POCTI/MGI/40844/2001)

Date: 2006   |   Origin: Repositório da Universidade de Lisboa
More info.
go first page go previous page
go to page: 1
go next page go last page
rss feed search results

2 Results

Queried text

Refine Results

Author





















Date



Document Type


Access rights



Resource



Subject