InterRett and RettBASE: International Rett Syndrome Association databases for Rett syndrome. (Q38425219)

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21 December 2019

title

InterRett and RettBASE: International Rett Syndrome Association databases for Rett syndrome (English)

1 reference

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21 December 2019

0 references

3

1 reference

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21 December 2019

author name string

Susan Fyfe

1

1 reference

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21 December 2019

Angela Cream

2

1 reference

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21 December 2019

John Christodoulou

4

1 reference

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21 December 2019

Helen Leonard

5

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21 December 2019

publication date

1 October 2003

1 reference

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Journal of Child Neurology

21 December 2019

published in

1 reference

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21 December 2019

volume

18

1 reference

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21 December 2019

issue

10

1 reference

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21 December 2019

page(s)

709-713

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Obtaining sensitive data through the Web: an example of design and methods

21 December 2019

cites work

1 reference

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Using the Internet to pilot a questionnaire on childhood disability in Rett syndrome

21 January 2018

1 reference

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Web-based administration of a personality questionnaire: comparison with traditional methods

21 January 2018

1 reference

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Online patient-helpers and physicians working together: a new partnership for high quality health care

21 January 2018

1 reference

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Describing the phenotype in Rett syndrome using a population database

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738030180100301

Medical aspects of school-aged children with Down syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738030180100301

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738030180100301

Rett syndrome: methyl-CpG-binding protein 2 mutations and phenotype-genotype correlations

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738030180100301

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/10.1177%2F08830738030180100301

Rett syndrome in Spain: mutation analysis and clinical correlations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738030180100301

Effects of MECP2 mutation type, location and X-inactivation in modulating Rett syndrome phenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738030180100301

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/10.1177%2F08830738030180100301

Associations between MeCP2 mutations, X-chromosome inactivation, and phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738030180100301

RettBASE: The IRSA MECP2 variation database-a new mutation database in evolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F08830738030180100301

10.1177/08830738030180100301

21 January 2018

Identifiers

DOI

1 reference

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21 December 2019

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