The Rett Syndrome Behaviour Questionnaire (RSBQ): refining the behavioural phenotype of Rett syndrome. (Q48436989)

11 February 2018

title

The Rett Syndrome Behaviour Questionnaire (RSBQ): refining the behavioural phenotype of Rett syndrome. (English)

1 reference

11 February 2018

1 reference

0 references

1 reference

3

1 reference

11 February 2018

Sheena Reilly

series ordinal

4

1 reference

11 February 2018

Hilary Cass

object named as

Hilary Cass

series ordinal

5

0 references

Tony Charman

series ordinal

2

object named as

Tony Charman

1 reference

11 February 2018

Rebecca H Mount

1

1 reference

11 February 2018

publication date

1 November 2002

1 reference

11 February 2018

The Journal of Child Psychology and Psychiatry

published in

1 reference

11 February 2018

volume

43

1 reference

11 February 2018

issue

8

1 reference

11 February 2018

page(s)

1099-1110

1 reference

11 February 2018

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

cites work

1 reference

https://api.crossref.org/works/10.1111%2F1469-7610.00236

MECP2 mutations account for most cases of typical forms of Rett syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2F1469-7610.00236

Psychiatric disorder in children with physical disabilities.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2F1469-7610.00236

Long-read sequence analysis of the MECP2 gene in Rett syndrome patients: correlation of disease severity with mutation type and location.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2F1469-7610.00236

Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2F1469-7610.00236

Rett syndrome: a surprising result of mutation in MECP2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2F1469-7610.00236

Population prevalence of psychopathology in children and adolescents with intellectual disability: I. Rationale and methods.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2F1469-7610.00236

Population prevalence of psychopathology in children and adolescents with intellectual disability: II. Epidemiological findings.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2F1469-7610.00236

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2F1469-7610.00236

Direct and indirect behavioral effects of different genetic disorders of mental retardation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2F1469-7610.00236

Rett syndrome: analysis of MECP2 and clinical characterization of 31 patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2F1469-7610.00236

Guidelines for reporting clinical features in cases with MECP2 mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2F1469-7610.00236

Quantifying the information value of clinical assessments with signal detection theory

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2F1469-7610.00236

Behavioural and emotional features in Rett syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2F1469-7610.00236

MECP2 mutations in Danish patients with Rett syndrome: high frequency of mutations but no consistent correlations with clinical severity or with the X chromosome inactivation pattern

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2F1469-7610.00236

21 January 2018

Identifiers

DOI

10.1111/1469-7610.00236

1 reference

11 February 2018

PubMed ID

12455930

1 reference

11 February 2018