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Beckwith–Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villi
Beckwith–Wiedemann syndrome (BWS) is an imprinting disorder that can be prenatally suspected or diagnosed based on established clinical guidelines. Molecular confirmation is commonly performed on amniocytes. The possibility to use fresh (CVF) and cultured (CVC) chorionic villi has never been investi...
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| Pubblicato in: | Epigenetics |
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| Autori principali: | , , , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Taylor & Francis
2015
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4622958/ https://ncbi.nlm.nih.gov/pubmed/26061650 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/15592294.2015.1057383 |
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