A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith–Wiedemann syndrome

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Bibliografski detalji
Izdano u:Proc Natl Acad Sci U S A
Glavni autori: Smilinich, Nancy J., Day, Colleen D., Fitzpatrick, Galina V., Caldwell, Germaine M., Lossie, Amy C., Cooper, P. R., Smallwood, Allan C., Joyce, Johanna A., Schofield, Paul N., Reik, Wolf, Nicholls, Robert D., Weksberg, Rosanna, Driscoll, D. J., Maher, Eamonn R., Shows, Thomas B., Higgins, Michael J.
Format: Artigo
Jezik:Inglês
Izdano: National Academy of Sciences 1999
Teme:
Biological Sciences
Online pristup:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC22188/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/10393948/
https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.96.14.8064
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