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

Year Number of Results
2002 1
2003 1
2005 1
2007 2
2008 2
2009 2
2010 7
2011 5
2012 1
2014 6
2015 6
2016 4
2017 2
2020 1
2021 1
2024 0

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38 results

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Page 1
Bone status in genetic syndromes: a review.
Stagi S, Iurato C, Lapi E, Cavalli L, Brandi ML, de Martino M. Stagi S, et al. Among authors: lapi e. Hormones (Athens). 2015 Jan-Mar;14(1):19-31. doi: 10.1007/BF03401378. Hormones (Athens). 2015. PMID: 25885101 Free article. Review.
Overlapping SETBP1 gain-of-function mutations in Schinzel-Giedion syndrome and hematologic malignancies.
Acuna-Hidalgo R, Deriziotis P, Steehouwer M, Gilissen C, Graham SA, van Dam S, Hoover-Fong J, Telegrafi AB, Destree A, Smigiel R, Lambie LA, Kayserili H, Altunoglu U, Lapi E, Uzielli ML, Aracena M, Nur BG, Mihci E, Moreira LM, Borges Ferreira V, Horovitz DD, da Rocha KM, Jezela-Stanek A, Brooks AS, Reutter H, Cohen JS, Fatemi A, Smitka M, Grebe TA, Di Donato N, Deshpande C, Vandersteen A, Marques Lourenço C, Dufke A, Rossier E, Andre G, Baumer A, Spencer C, McGaughran J, Franke L, Veltman JA, De Vries BB, Schinzel A, Fisher SE, Hoischen A, van Bon BW. Acuna-Hidalgo R, et al. Among authors: lapi e. PLoS Genet. 2017 Mar 27;13(3):e1006683. doi: 10.1371/journal.pgen.1006683. eCollection 2017 Mar. PLoS Genet. 2017. PMID: 28346496 Free PMC article.
Bone Mineral Status in Children and Adolescents with Klinefelter Syndrome.
Stagi S, Di Tommaso M, Manoni C, Scalini P, Chiarelli F, Verrotti A, Lapi E, Giglio S, Dosa L, de Martino M. Stagi S, et al. Among authors: lapi e. Int J Endocrinol. 2016;2016:3032759. doi: 10.1155/2016/3032759. Epub 2016 Jun 16. Int J Endocrinol. 2016. PMID: 27413371 Free PMC article.
38 results