Beckwith–Wiedemann syndrome and uniparental disomy 11p: fine mapping of the recombination breakpoints and evaluation of several techniques

MLA

Esther Gean, et al. “Beckwith–Wiedemann Syndrome and Uniparental Disomy 11p: Fine Mapping of the Recombination Breakpoints and Evaluation of Several Techniques.” European Journal of Human Genetics, vol. 19, Jan. 2011, pp. 416–21. EBSCOhost, https://doi.org/10.1038/ejhg.2010.236.

APA

Esther Gean, Victor Martinez-Glez, Ricardo Gracia-Bouthelier, Encarna Guillén, Loreto Martorell, Julián Nevado, Sixto García-Miñaur, Mario F. Fraga, Victoria Esteban Marfil, Pablo Lapunzina, Luis Morís Fernández, Heloisa Meneses, & Valeria Romanelli. (2011). Beckwith–Wiedemann syndrome and uniparental disomy 11p: fine mapping of the recombination breakpoints and evaluation of several techniques. European Journal of Human Genetics, 19, 416–421. https://doi.org/10.1038/ejhg.2010.236

Chicago

Esther Gean, Victor Martinez-Glez, Ricardo Gracia-Bouthelier, Encarna Guillén, Loreto Martorell, Julián Nevado, Sixto García-Miñaur, et al. 2011. “Beckwith–Wiedemann Syndrome and Uniparental Disomy 11p: Fine Mapping of the Recombination Breakpoints and Evaluation of Several Techniques.” European Journal of Human Genetics 19 (January): 416–21. doi:10.1038/ejhg.2010.236.