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...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7583213/
https://www.ncbi.nlm.nih.gov/pubmed/33092629
http://dx.doi.org/10.1186/s13148-020-00949-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7583213/
https://www.ncbi.nlm.nih.gov/pubmed/33092629
http://dx.doi.org/10.1186/s13148-020-00949-8

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