Publications

Rett Syndrome with and Without Detected Mecp2 Mutations: An Attempt to Redefine Phenotypes

AuthID
P-002-Y4P

Author(s)

Temudo, T

Santos, M

Ramos, E

Dias, K

Vieira, JP

Moreira, A

Calado, E

Carrilho, I

Oliveira, G

Levy, A

Barbot, C

[+4]·

Borges, L

Gomes, R

Mira, G

Pereira, SA

Santos, M

Epplen, JT

Document Type

Article

Year published

2011

Published

in BRAIN & DEVELOPMENT, ISSN: 0387-7604

Volume: 33, Issue: 1, Pages: 69-76 (8)

Indexing

Wos^®

Scopus^®

Crossref^®

Pubmed^®

Handle^®

Google Scholar^®

Metadata
Sources

Publication Identifiers

DOI: 10.1016/j.braindev.2010.01.004

Handle: https://hdl.handle.net/1822/19077

Pubmed: 20116947

Scopus: 2-s2.0-78650306582

Wos: WOS:000286910700011

Source Identifiers

ISSN: 0387-7604

Export Publication Metadata

Marked List

Add to Marked List

Info

At this moment we don't have any links to full text documens.

All authors

Name Order	Name	Name Order	Name	Name Order	Name
1	Temudo, T;	2	Santos, M;	3	Ramos, E ;
4	Dias, K;	5	Vieira, JP;	6	Moreira, A;
7	Calado, E;	8	Carrilho, I;	9	Oliveira, G ;
10	Levy, A;	11	Barbot, C ;	12	Fonseca, M;
13	Cabral, A;	14	Cabral, P;	15	Monteiro, J;
16	Borges, L;	17	Gomes, R;	18	Mira, G;
19	Pereira, SA;	20	Santos, M;	21	Fernandes, A ;
22	Epplen, JT;	23	Sequeiros, J ;	24	Maciel, P ;

Rett Syndrome with and Without Detected Mecp2 Mutations: An Attempt to Redefine Phenotypes

Useful Links

Get Help

Federated Authentication (Click on the image)

Rett Syndrome with and Without Detected Mecp2 Mutations: An Attempt to Redefine Phenotypes

Useful Links

Get Help