(Q50310996)

English

Rett syndrome: prevalence among Chinese and a comparison of MECP2 mutations of classic Rett syndrome with other neurodevelopmental disorders.

scientific article published in December 2007

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/18174559

Rett syndrome: prevalence among Chinese and a comparison of MECP2 mutations of classic Rett syndrome with other neurodevelopmental disorders. (English)

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/18174559

neurodevelopmental disorder

1 reference

based on heuristic

inferred from title

0 references

author name string

Virginia C N Wong

1

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/18174559

Susanna Y H Li

2

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/18174559

publication date

1 December 2007

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/18174559

Journal of Child Neurology

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/18174559

22

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/18174559

12

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/18174559

1397-1400

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/18174559

Rett's syndrome: prevalence and impact on progressive severe mental retardation in girls

1 reference

https://api.crossref.org/works/10.1177%2F0883073807307091

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1177%2F0883073807307091

21 January 2018

Methyl-CpG binding protein 2 gene (MECP2) variations in Japanese patients with Rett syndrome: pathological mutations and polymorphisms.

1 reference

https://api.crossref.org/works/10.1177%2F0883073807307091

21 January 2018

Rett syndrome: new clinical and molecular insights.

1 reference

https://api.crossref.org/works/10.1177%2F0883073807307091

21 January 2018

A mutation hot spot for nonspecific X-linked mental retardation in the MECP2 gene causes the PPM-X syndrome

1 reference

https://api.crossref.org/works/10.1177%2F0883073807307091

21 January 2018

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders

1 reference

https://api.crossref.org/works/10.1177%2F0883073807307091

21 January 2018

Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome

1 reference

https://api.crossref.org/works/10.1177%2F0883073807307091

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1177%2F0883073807307091

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1177%2F0883073807307091

21 January 2018

Rett syndrome: geographic variation in prevalence in Norway.

1 reference

https://api.crossref.org/works/10.1177%2F0883073807307091

21 January 2018

Screening for MECP2 mutations in Spanish patients with an unexplained mental retardation.

1 reference

https://api.crossref.org/works/10.1177%2F0883073807307091

21 January 2018

A new cohort of MECP2 mutation screening in unexplained mental retardation: careful re-evaluation is the best indicator for molecular diagnosis.

1 reference

https://api.crossref.org/works/10.1177%2F0883073807307091

21 January 2018

Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males.

1 reference

https://api.crossref.org/works/10.1177%2F0883073807307091

21 January 2018

Identifiers

10.1177/0883073807307091

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/18174559

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

2 March 2018

http://europepmc.org/abstract/MED/18174559

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q50310996&oldid=1431427566"