(Q40137142)

17 September 2017

Rett syndrome: North American database (English)

1 reference

17 September 2017

1 reference

Patrick MacLeod

9

0 references

Alan K. Percy

1

object named as

Alan K Percy

1 reference

17 September 2017

8

Daniel G Glaze

1 reference

17 September 2017

Jane B Lane

2

1 reference

17 September 2017

Jerry Childers

3

1 reference

17 September 2017

Steve Skinner

4

1 reference

17 September 2017

Fran Annese

5

1 reference

17 September 2017

Judy Barrish

6

1 reference

17 September 2017

Erwin Caeg

7

1 reference

17 September 2017

1 December 2007

1 reference

Journal of Child Neurology

17 September 2017

1 reference

17 September 2017

22

1 reference

17 September 2017

12

1 reference

17 September 2017

1338-1341

1 reference

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

17 September 2017

1 reference

https://api.crossref.org/works/10.1177%2F0883073807308715

Rett syndrome: model of neurodevelopmental disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807308715

Rett syndrome in Australia: a review of the epidemiology.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807308715

Diagnostic testing for Rett syndrome by DHPLC and direct sequencing analysis of the MECP2 gene: identification of several novel mutations and polymorphisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807308715

Rett syndrome in Spain: mutation analysis and clinical correlations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807308715

Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807308715

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%2F0883073807308715

MECP2 gene mutation analysis in Chinese patients with Rett syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807308715

Italian Rett database and biobank.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807308715

Mutation analysis of the MECP2 gene in patients of Slavic origin with Rett syndrome: novel mutations and polymorphisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073807308715

21 January 2018

Identifiers

DOI

10.1177/0883073807308715

1 reference

17 September 2017

1 reference