(Q30354004)

20 June 2017

People with MECP2 mutation-positive Rett disorder who converse. (English)

1 reference

20 June 2017

Kerr AM

1

1 reference

20 June 2017

Archer HL

2

1 reference

20 June 2017

Evans JC

3

1 reference

20 June 2017

Prescott RJ

4

1 reference

20 June 2017

Gibbon F

5

1 reference

20 June 2017

1 May 2006

1 reference

Journal of Intellectual Disability Research

20 June 2017

1 reference

20 June 2017

50

1 reference

20 June 2017

386-394

1 reference

20 June 2017

Pt 5

1 reference

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

20 June 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2005.00786.X

Neuropathology of Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2005.00786.X

Morphological study of neocortical areas in Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2005.00786.X

Nurse recognition of early deviation in development in home videos of infants with Rett disorder.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2005.00786.X

Refining the phenotype of common mutations in Rett syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2005.00786.X

A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2005.00786.X

Rett variants: a suggested model for inclusion criteria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2005.00786.X

Guidelines for reporting clinical features in cases with MECP2 mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2005.00786.X

Mind and brain in Rett disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2005.00786.X

Functional analyses of MeCP2 mutations associated with Rett syndrome using transient expression systems.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2005.00786.X

Patients with the R133C mutation: is their phenotype different from patients with Rett syndrome with other mutations?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2005.00786.X

Chromosome 2 deletion encompassing the MAP2 gene in a patient with autism and Rett-like features.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2005.00786.X

Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2005.00786.X

Multiple pathways regulate MeCP2 expression in normal brain development and exhibit defects in autism-spectrum disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2005.00786.X

X-chromosome inactivation patterns are unbalanced and affect the phenotypic outcome in a mouse model of rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2005.00786.X

The Rett girls with preserved speech

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2788.2005.00786.X

10.1111/J.1365-2788.2005.00786.X

21 January 2018

Identifiers

DOI

1 reference

20 June 2017

1 reference