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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2003 1
2006 2
2007 2
2008 1
2014 1
2015 2
2016 3
2017 1
2018 1
2019 6
2020 5
2022 1
2024 0

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24 results

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Page 1
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
Heterozygous rare genetic variants in non-syndromic early-onset obesity.
Serra-Juhé C, Martos-Moreno GÁ, Bou de Pieri F, Flores R, Chowen JA, Pérez-Jurado LA, Argente J. Serra-Juhé C, et al. Among authors: flores r. Int J Obes (Lond). 2020 Apr;44(4):830-841. doi: 10.1038/s41366-019-0357-5. Epub 2019 Mar 29. Int J Obes (Lond). 2020. PMID: 30926952 Free PMC article.
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.
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.
24 results