×
Entrez Id:
2290
Gene Symbol:
FOXG1
FOXG1
FOXG1 syndrome
0.790
CausalMutation
CLINVAR
Novel FOXG1 mutations in Chinese patients with Rett syndrome or Rett-like mental retardation.
28851325
2017
×
Entrez Id:
2290
Gene Symbol:
FOXG1
FOXG1
FOXG1 syndrome
0.790
CausalMutation
CLINVAR
The hyperkinetic movement disorder of FOXG1-related epileptic-dyskinetic encephalopathy.
26344814
2016
×
Entrez Id:
2290
Gene Symbol:
FOXG1
FOXG1
FOXG1 syndrome
0.790
CausalMutation
CLINVAR
Delineation of the movement disorders associated with FOXG1 mutations.
27029630
2016
×
Entrez Id:
2290
Gene Symbol:
FOXG1
FOXG1
FOXG1 syndrome
0.790
GeneticVariation
CLINVAR
A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders.
26938784
2016
×
Entrez Id:
2290
Gene Symbol:
FOXG1
FOXG1
FOXG1 syndrome
0.790
CausalMutation
CLINVAR
De novo mutations in moderate or severe intellectual disability.
25356899
2014
×
Entrez Id:
2290
Gene Symbol:
FOXG1
FOXG1
FOXG1 syndrome
0.790
CausalMutation
CLINVAR
The usefulness of whole-exome sequencing in routine clinical practice.
24901346
2014
×
Entrez Id:
2290
Gene Symbol:
FOXG1
FOXG1
FOXG1 syndrome
0.790
CausalMutation
CLINVAR
Epilepsy and outcome in FOXG1-related disorders.
24836831
2014
×
Entrez Id:
2290
Gene Symbol:
FOXG1
FOXG1
FOXG1 syndrome
0.790
CausalMutation
CLINVAR
Expanding the phenotype associated with FOXG1 mutations and in vivo FoxG1 chromatin-binding dynamics.
22091895
2012
×
Entrez Id:
2290
Gene Symbol:
FOXG1
FOXG1
FOXG1 syndrome
0.790
CausalMutation
CLINVAR
14q12 and severe Rett-like phenotypes: new clinical insights and physical mapping of FOXG1-regulatory elements.
22739344
2012
×
Entrez Id:
2290
Gene Symbol:
FOXG1
FOXG1
FOXG1 syndrome
0.790
CausalMutation
CLINVAR
Submicroscopic deletions in 14q12 spanning FOXG1 or intragenic mutations have been reported in patients with a developmental disorder described as a congenital variant of Rett syndrome .
21441262
2011
×
Entrez Id:
2290
Gene Symbol:
FOXG1
FOXG1
FOXG1 syndrome
0.790
CausalMutation
CLINVAR
The forkhead box G1 (FOXG1 )gene has recently been associated with the congenital variant of Rett syndrome , and so far 17 mutations have been reported.
21280142
2011
×
Entrez Id:
2290
Gene Symbol:
FOXG1
FOXG1
FOXG1 syndrome
0.790
CausalMutation
CLINVAR
Phenotypic variability in Rett syndrome associated with FOXG1 mutations in females.
19564653
2010
×
Entrez Id:
2290
Gene Symbol:
FOXG1
FOXG1
FOXG1 syndrome
0.790
CausalMutation
CLINVAR
Revisiting the phenotype associated with FOXG1 mutations: two novel cases of congenital Rett variant.
19806373
2010
×
Entrez Id:
2290
Gene Symbol:
FOXG1
FOXG1
FOXG1 syndrome
0.790
CausalMutation
CLINVAR
Here, we report the identification of FOXG1 -truncating mutations in two patients affected by the congenital variant of Rett syndrome .
18571142
2008