Rett syndrome with and without detected MECP2 mutations: an attempt to redefine phenotypes.
about
Quantification of functional abilities in Rett syndrome: a comparison between stages III and IVOligodendrocyte lineage cells contribute unique features to Rett syndrome neuropathologyThe role of oxidative stress in Rett syndrome: an overview.Treatment of behavioral problems in intellectually disabled adult patients with epilepsy.Rett syndrome and MeCP2.Xq28 (MECP2) microdeletions are common in mutation-negative females with Rett syndrome and cause mild subtypes of the diseaseComparing social reciprocity in preserved speech variant and typical Rett syndrome during the early years of life.Neurodevelopmental disorders: Clinical criteria for Rett syndrome.
P2860
Q33863430-38439943-8C5F-43FE-8725-2FF85B1C787DQ37345132-593D4FC1-27CF-425C-B684-2F4022AEB6B9Q38023570-2C057E21-58B6-4D85-A614-8FC9E7FFF43AQ38086302-11ED2EAC-AEB5-4894-B8D9-489F57CEDBC7Q38194967-5ABD0AD9-89E7-4E50-BD4F-AC5C8C3325E2Q42089130-AA09FC57-ADB4-4646-A2DD-23BE10C83E73Q48087635-048D8322-7D03-4B32-9ADC-9F7564AEB893Q54589200-CD47BA59-2E7B-4F11-8D41-F2C5D43F3A22
P2860
Rett syndrome with and without detected MECP2 mutations: an attempt to redefine phenotypes.
description
2010 nî lūn-bûn
@nan
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
2010年论文
@zh
2010年论文
@zh-cn
name
Rett syndrome with and without ...... ttempt to redefine phenotypes.
@en
type
label
Rett syndrome with and without ...... ttempt to redefine phenotypes.
@en
prefLabel
Rett syndrome with and without ...... ttempt to redefine phenotypes.
@en
P2093
P50
P1476
Rett syndrome with and without ...... attempt to redefine phenotypes
@en
P2093
Alexandra Cabral
Ana Moreira
António Levy
Eulália Calado
Graça Mira
Inês Carrilho
José Monteiro
José Pedro Vieira
Karin Dias
Luís Borges
P356
10.1016/J.BRAINDEV.2010.01.004
P50
P577
2010-02-08T00:00:00Z