Llwytho...
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...
Wedi'i Gadw mewn:
| Cyhoeddwyd yn: | Clin Epigenetics |
|---|---|
| Prif Awduron: | , , , , , , , , , , , |
| Fformat: | Artigo |
| Iaith: | Inglês |
| Cyhoeddwyd: |
BioMed Central
2020
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| Pynciau: | |
| Mynediad Ar-lein: | 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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