Different Mechanisms Cause Hypomethylation of Both
11p15.5 imprinted genes cluster
DNA methylation defects
Silver–Russell syndrome
differentially methylated regions
imprinting disorders
microduplication
Journal
Genes
ISSN: 2073-4425
Titre abrégé: Genes (Basel)
Pays: Switzerland
ID NLM: 101551097
Informations de publication
Date de publication:
16 10 2022
16 10 2022
Historique:
received:
10
08
2022
revised:
27
09
2022
accepted:
13
10
2022
entrez:
27
10
2022
pubmed:
28
10
2022
medline:
29
10
2022
Statut:
epublish
Résumé
Silver-Russell syndrome is an imprinting disorder characterised by pre- and post-natal growth retardation and several heterogeneous molecular defects affecting different human genomic loci. In the majority of cases, the molecular defect is the loss of methylation (LOM) of the
Identifiants
pubmed: 36292759
pii: genes13101875
doi: 10.3390/genes13101875
pmc: PMC9602374
pii:
doi:
Types de publication
Case Reports
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
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