(Q34460607)

2 August 2017

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title

Rett syndrome: clinical correlates of the newly discovered gene (English)

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2 August 2017

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Percy AK

1

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2 August 2017

publication date

1 December 2001

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2 August 2017

published in

Brain and Development

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2 August 2017

volume

23 Suppl 1

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2 August 2017

page(s)

S202-5

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A progressive syndrome of autism, dementia, ataxia, and loss of purposeful hand use in girls: Rett's syndrome: report of 35 cases

2 August 2017

cites work

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https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900350-3

7 January 2021

Diagnostic criteria for Rett syndrome. The Rett Syndrome Diagnostic Criteria Work Group

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https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900350-3

7 January 2021

Rett variants: a suggested model for inclusion criteria.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900350-3

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900350-3

7 January 2021

Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes

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https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900350-3

7 January 2021

Rett syndrome and beyond: recurrent spontaneous and familial MECP2 mutations at CpG hotspots

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https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900350-3

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900350-3

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900350-3

7 January 2021

Mutation screening in Rett syndrome patients.

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https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900350-3

7 January 2021

Rett syndrome in a boy with a 47,XXY karyotype

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https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900350-3

7 January 2021

Somatic mutation in MECP2 as a non-fatal neurodevelopmental disorder in males

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https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900350-3

7 January 2021

Preserved speech variant is allelic of classic Rett syndrome

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https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900350-3

7 January 2021

A mutation in the rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in males

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900350-3

7 January 2021

Neonatal encephalopathy in two boys in families with recurrent Rett syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900350-3

7 January 2021

Decreased dendritic branching in frontal, motor and limbic cortex in Rett syndrome compared with trisomy 21.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2801%2900350-3

7 January 2021

10.1016/S0387-7604(01)00350-3

Identifiers

DOI

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2 August 2017

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