Beckwith–Wiedemann syndrome and uniparental disomy 11p: fine mapping of the recombination breakpoints and evaluation of several techniques
- DOI
- 10.1038/ejhg.2010.236
- Published
- 2011-01-19
- 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.2010.236,
title = {Beckwith–Wiedemann syndrome and uniparental disomy 11p: fine mapping of the recombination breakpoints and evaluation of several techniques},
author = {Valeria Romanelli and Heloisa N M Meneses and Luis Fernández and Victor Martínez-Glez and Ricardo Gracia-Bouthelier and Mario F Fraga and Encarna Guillén and Julián Nevado and Esther Gean and Loreto Martorell and Victoria Esteban Marfil and Sixto García-Miñaur and Pablo Lapunzina},
year = {2011},
journal = {European Journal of Human Genetics},
doi = {10.1038/ejhg.2010.236},
url = {https://doi.org/10.1038/ejhg.2010.236}
}RIS
TY - JOUR TI - Beckwith–Wiedemann syndrome and uniparental disomy 11p: fine mapping of the recombination breakpoints and evaluation of several techniques AU - Valeria Romanelli AU - Heloisa N M Meneses AU - Luis Fernández AU - Victor Martínez-Glez AU - Ricardo Gracia-Bouthelier AU - Mario F Fraga AU - Encarna Guillén AU - Julián Nevado AU - Esther Gean AU - Loreto Martorell AU - Victoria Esteban Marfil AU - Sixto García-Miñaur AU - Pablo Lapunzina PY - 2011 JO - European Journal of Human Genetics DO - 10.1038/ejhg.2010.236 UR - https://doi.org/10.1038/ejhg.2010.236 ER -
APA
Romanelli, V., Meneses, H. N. M., Fernández, L., Martínez-Glez, V., Gracia-Bouthelier, R., Fraga, M. F., Guillén, E., Nevado, J., Gean, E., Martorell, L., Marfil, V. E., García-Miñaur, S., & Lapunzina, P. (2011). Beckwith–Wiedemann syndrome and uniparental disomy 11p: fine mapping of the recombination breakpoints and evaluation of several techniques. European Journal of Human Genetics. https://doi.org/10.1038/ejhg.2010.236
Source records
- crossref · retrieved 2026-09-25T03:28:58.930Z