A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith–Wiedemann syndrome
- DOI
- 10.1038/ejhg.2016.3
- Published
- 2016-02-03
- Container
- European Journal of Human Genetics
- Publisher
- Springer Science and Business Media LLC
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1038/ejhg.2016.3,
title = {A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith–Wiedemann syndrome},
author = {Jasmin Beygo and Ivana Joksic and Tim M Strom and Hermann-Josef Lüdecke and Julia Kolarova and Reiner Siebert and Zeljko Mikovic and Bernhard Horsthemke and Karin Buiting},
year = {2016},
journal = {European Journal of Human Genetics},
doi = {10.1038/ejhg.2016.3},
url = {https://doi.org/10.1038/ejhg.2016.3}
}RIS
TY - JOUR TI - A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith–Wiedemann syndrome AU - Jasmin Beygo AU - Ivana Joksic AU - Tim M Strom AU - Hermann-Josef Lüdecke AU - Julia Kolarova AU - Reiner Siebert AU - Zeljko Mikovic AU - Bernhard Horsthemke AU - Karin Buiting PY - 2016 JO - European Journal of Human Genetics DO - 10.1038/ejhg.2016.3 UR - https://doi.org/10.1038/ejhg.2016.3 ER -
APA
Beygo, J., Joksic, I., Strom, T. M., Lüdecke, H., Kolarova, J., Siebert, R., Mikovic, Z., Horsthemke, B., & Buiting, K. (2016). A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith–Wiedemann syndrome. European Journal of Human Genetics. https://doi.org/10.1038/ejhg.2016.3
Source records
- crossref · retrieved 2026-11-09T16:13:12.997Z