(Q41934633)

14 October 2017

title

FOXG1 mutations in Japanese patients with the congenital variant of Rett syndrome (English)

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14 October 2017

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S Takahashi

1

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N Matsumoto

2

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A Okayama

3

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N Suzuki

4

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A Araki

5

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K Okajima

6

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H Tanaka

7

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A Miyamoto

8

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14 October 2017

publication date

16 December 2011

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14 October 2017

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14 October 2017

volume

82

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issue

6

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14 October 2017

page(s)

569-573

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Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2

14 October 2017

cites work

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https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01819.X

Rett syndrome: revised diagnostic criteria and nomenclature

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01819.X

Rett variants: a suggested model for inclusion criteria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01819.X

Rett syndrome and the MECP2 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01819.X

Haploinsufficiency of novel FOXG1B variants in a patient with severe mental retardation, brain malformations and microcephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01819.X

Additional chromosomal abnormalities in patients with a previously detected abnormal karyotype, mental retardation, and dysmorphic features.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01819.X

Atypical Rett syndrome with selective FOXG1 deletion detected by comparative genomic hybridization: case report and review of literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01819.X

14q12 Microdeletion syndrome and congenital variant of Rett syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01819.X

Winged helix transcription factor BF-1 is essential for the development of the cerebral hemispheres

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01819.X

Foxg1 suppresses early cortical cell fate

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01819.X

The timing of cortical neurogenesis is encoded within lineages of individual progenitor cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01819.X

Disruption of Foxg1 expression by knock-in of cre recombinase: effects on the development of the mouse telencephalon

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01819.X

FOXG1 is responsible for the congenital variant of Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01819.X

Revisiting the phenotype associated with FOXG1 mutations: two novel cases of congenital Rett variant

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01819.X

Novel FOXG1 mutations associated with the congenital variant of Rett syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01819.X

Phenotypic variability in Rett syndrome associated with FOXG1 mutations in females.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01819.X

The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01819.X

A missense mutation within the fork-head domain of the forkhead box G1 Gene (FOXG1) affects its nuclear localization

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01819.X

A FOXG1 mutation in a boy with congenital variant of Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01819.X

The winged-helix protein brain factor 1 interacts with groucho and hes proteins to repress transcription

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2011.01819.X

10.1111/J.1399-0004.2011.01819.X

21 January 2018

Identifiers

DOI

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14 October 2017

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