Genome-wide methylation analysis in Silver–Russell syndrome, Temple syndrome, and Prader–Willi syndrome

BACKGROUND: Imprinting disorders (IDs) show overlapping phenotypes, particularly in Silver–Russell syndrome (SRS), Temple syndrome (TS14), and Prader–Willi syndrome (PWS). These three IDs include fetal and postnatal growth failure, feeding difficulty, and muscular hypotonia as major clinical feature...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:Clin Epigenetics
Egile Nagusiak: Hara-Isono, Kaori, Matsubara, Keiko, Fuke, Tomoko, Yamazawa, Kazuki, Satou, Kazuhito, Murakami, Nobuyuki, Saitoh, Shinji, Nakabayashi, Kazuhiko, Hata, Kenichiro, Ogata, Tsutomu, Fukami, Maki, Kagami, Masayo
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2020
Gaiak:
Research
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC7583213/
https://ncbi.nlm.nih.gov/pubmed/33092629
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13148-020-00949-8
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