Male Rett syndrome variant: application of diagnostic criteria.

Male Rett syndrome variant: application of diagnostic criteria.

Item
http://www.wikidata.org/entity/Q33596633
Rett syndrome: a prototypical neurodevelopmental disorderThe phenotypic consequences of MECP2 mutations extend beyond Rett syndrome.Associations between MeCP2 mutations, X-chromosome inactivation, and phenotype.Rapid genotyping of common MeCP2 mutations with an electronic DNA microchip using serial differential hybridizationMeCP2-Related Diseases and Animal Models.Microglia as modulators of cognition and neuropsychiatric disorders.Rett syndrome and MeCP2.Brief report: systematic review of Rett syndrome in males.Rett syndrome: clinical manifestations in males with MECP2 mutations.Occurrence of Rett syndrome in boys.Polymorphisms in the C-terminal domain of MECP2 in mentally handicapped boys: implications for genetic counselling.Transcriptome level analysis in Rett syndrome using human samples from different tissues.
P2860

Male Rett syndrome variant: application of diagnostic criteria.

Item
http://www.wikidata.org/entity/Q33596633
description
1999 nî lūn-bûn
@nan
1999 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի մարտին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Male Rett syndrome variant: application of diagnostic criteria.
@ast
Male Rett syndrome variant: application of diagnostic criteria.
@en
type
label
Male Rett syndrome variant: application of diagnostic criteria.
@ast
Male Rett syndrome variant: application of diagnostic criteria.
@en
prefLabel
Male Rett syndrome variant: application of diagnostic criteria.
@ast
Male Rett syndrome variant: application of diagnostic criteria.
@en
P1433
P1476
P2093
P304
P31
P356
P433
P478
P577
P5875
P698
P356
P1433
P1476
Male Rett syndrome variant: application of diagnostic criteria.
@en
P2093
P304
P31
P356
10.1016/S0887-8994(98)00150-7
P433
P478
P577
P5875
P698