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Fetal growth restriction in a genetic model of sporadic Beckwith–Wiedemann syndrome
Beckwith–Wiedemann syndrome (BWS) is a complex imprinting disorder involving fetal overgrowth and placentomegaly, and is associated with a variety of genetic and epigenetic mutations affecting the expression of imprinted genes on human chromosome 11p15.5. Most BWS cases are linked to loss of methyla...
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| Опубликовано в: : | Dis Model Mech |
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| Главные авторы: | , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
The Company of Biologists Ltd
2018
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6262809/ https://ncbi.nlm.nih.gov/pubmed/30158284 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.035832 |
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