Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutations.

Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutations.

Item
http://www.wikidata.org/entity/Q41134121
Rett syndrome and MeCP2: linking epigenetics and neuronal functionRett syndrome.Linkage analysis in Rett syndrome families suggests that there may be a critical region at Xq28Molecular approaches to the Rett syndrome gene.Genetic basis of Rett syndrome.Associations between MeCP2 mutations, X-chromosome inactivation, and phenotype.Examination of X chromosome markers in Rett syndrome: exclusion mapping with a novel variation on multilocus linkage analysisA new Rett syndrome family consistent with X-linked inheritance expands the X chromosome exclusion map.MicroRNAs in psychiatric and neurodevelopmental disorders.Exclusion of the gastrin-releasing peptide receptor (GRPR) locus as a candidate gene for Rett syndrome.Distinct de novo deletions in a brother-sister pair with RTT: a case report.Familial aggregation in Rett syndrome: what is the evidence for clustering of other disorders in families of affected girls?
P2860

Rett syndrome: exclusion mapping following the hypothesis of germinal mosaicism for new X-linked mutations.

Item
http://www.wikidata.org/entity/Q41134121
description
1991 nî lūn-bûn
@nan
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
1991年论文
@zh
1991年论文
@zh-cn
name
Rett syndrome: exclusion mappi ...... sm for new X-linked mutations.
@en
type
label
Rett syndrome: exclusion mappi ...... sm for new X-linked mutations.
@en
prefLabel
Rett syndrome: exclusion mappi ...... sm for new X-linked mutations.
@en
P1433
P1476
P2093
P2888
P304
P31
P356
P433
P478
P577
P6179
P698
P356
P1433
P1476
Rett syndrome: exclusion mappi ...... sm for new X-linked mutations.
@en
P2093
P2888
P304
P31
P356
P433
P478
P577
P6179
P698