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Mutational mechanisms of Williams-Beuren syndrome deletions.
Bayés M, Magano LF, Rivera N, Flores R, Pérez Jurado LA. Bayés M, et al. Among authors: flores r. Am J Hum Genet. 2003 Jul;73(1):131-51. doi: 10.1086/376565. Epub 2003 Jun 9. Am J Hum Genet. 2003. PMID: 12796854 Free PMC article.
[Williams syndrome: its clinical aspects and molecular bases].
Antonell A, Del Campo M, Flores R, Campuzano V, Perez-Jurado LA. Antonell A, et al. Among authors: flores r. Rev Neurol. 2006 Jan 7;42 Suppl 1:S69-75. Rev Neurol. 2006. PMID: 16506136 Free article. Review. Spanish.
Metabolic abnormalities in Williams-Beuren syndrome.
Palacios-Verdú MG, Segura-Puimedon M, Borralleras C, Flores R, Del Campo M, Campuzano V, Pérez-Jurado LA. Palacios-Verdú MG, et al. Among authors: flores r. J Med Genet. 2015 Apr;52(4):248-55. doi: 10.1136/jmedgenet-2014-102713. Epub 2015 Feb 6. J Med Genet. 2015. PMID: 25663682
Association of common copy number variants at the glutathione S-transferase genes and rare novel genomic changes with schizophrenia.
Rodríguez-Santiago B, Brunet A, Sobrino B, Serra-Juhé C, Flores R, Armengol L, Vilella E, Gabau E, Guitart M, Guillamat R, Martorell L, Valero J, Gutiérrez-Zotes A, Labad A, Carracedo A, Estivill X, Pérez-Jurado LA. Rodríguez-Santiago B, et al. Among authors: flores r. Mol Psychiatry. 2010 Oct;15(10):1023-33. doi: 10.1038/mp.2009.53. Epub 2009 Jun 16. Mol Psychiatry. 2010. PMID: 19528963
DNA methylation abnormalities in congenital heart disease.
Serra-Juhé C, Cuscó I, Homs A, Flores R, Torán N, Pérez-Jurado LA. Serra-Juhé C, et al. Among authors: flores r. Epigenetics. 2015;10(2):167-77. doi: 10.1080/15592294.2014.998536. Epigenetics. 2015. PMID: 25587870 Free PMC article.
1,275 results