7 Article(s)Download |
PMID | Title | Pub. Year | #Total Relationships |
1 | 29212017 | Control of Huntington's Disease-Associated Phenotypes by the Striatum-Enriched Transcription Factor Foxp2. | 2017 Dec 5 | 1 |
2 | 27933109 | Functional characterization of rare FOXP2 variants in neurodevelopmental disorder. | 2016 | 2 |
3 | 26497390 | Contactin‑associated protein‑like 2 expression in SH‑SY5Y cells is upregulated by a FOXP2 mutant with a shortened poly‑glutamine tract. | 2015 Dec | 3 |
4 | 15737702 | Absence of causative mutations and presence of autism-related allele in FOXP2 in Japanese autistic patients. | 2005 Apr | 1 |
5 | 15108192 | Association between the FOXP2 gene and autistic disorder in Chinese population. | 2004 May 15 | 1 |
6 | 11894222 | FOXP2 is not a major susceptibility gene for autism or specific language impairment. | 2002 May | 2 |
7 | 10880297 | The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder. | 2000 Aug | 1 |