(Q47220197)

12 January 2018

title

Rett syndrome: clinical and epidemiological aspects in a Brazilian institution (English)

1 reference

12 January 2018

1 reference

Cristina M Pozzi

1

1 reference

12 January 2018

Sergio Rosemberg

series ordinal

2

1 reference

12 January 2018

publication date

1 December 2003

1 reference

12 January 2018

Arquivos de Neuro-Psiquiatria

published in

1 reference

12 January 2018

volume

61

1 reference

12 January 2018

issue

4

1 reference

12 January 2018

page(s)

909-915

1 reference

12 January 2018

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

cites work

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2003000600004

Rett syndrome: clinical peculiarities and biological mysteries

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2003000600004

[Rett's syndrome: analysis of the 1st 5 cases diagnosed in Brazil]

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2003000600004

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/10.1590%2FS0004-282X2003000600004

Rett syndrome and the MECP2 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2003000600004

Molecular genetics of Rett syndrome and clinical spectrum of MECP2 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2003000600004

Rett variants: a suggested model for inclusion criteria.

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2003000600004

The Rett girls with preserved speech

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2003000600004

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2003000600004

Rett syndrome: clinical correlates of the newly discovered gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2003000600004

MECP2 is highly mutated in X-linked mental retardation

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2003000600004

Rett syndrome studies of natural history and search for a genetic marker

21 January 2018

1 reference

https://api.crossref.org/works/10.1590%2FS0004-282X2003000600004

10.1590/S0004-282X2003000600004

21 January 2018

Identifiers

DOI

1 reference

12 January 2018

1 reference

12 January 2018