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

Year Number of Results
2009 2
2010 1
2011 4
2012 1
2014 1
2015 3
2016 3
2017 3
2018 3
2019 2
2020 3
2021 0
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24 results
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Page 1
A novel MED12 mutation: Evidence for a fourth phenotype.
Prontera P, Ottaviani V, Rogaia D, Isidori I, Mencarelli A, Malerba N, Cocciadiferro D, Rolph P, Stangoni G, Vulto-van Silfhout A, Merla G. Prontera P, et al. Among authors: stangoni g. Am J Med Genet A. 2016 Sep;170(9):2377-82. doi: 10.1002/ajmg.a.37805. Epub 2016 Jun 17. Am J Med Genet A. 2016. PMID: 27312080 Review.
Deletion 2p15-16.1 syndrome: case report and review.
Prontera P, Bernardini L, Stangoni G, Capalbo A, Rogaia D, Romani R, Ardisia C, Dallapiccola B, Donti E. Prontera P, et al. Among authors: stangoni g. Am J Med Genet A. 2011 Oct;155A(10):2473-8. doi: 10.1002/ajmg.a.33875. Epub 2011 Sep 9. Am J Med Genet A. 2011. PMID: 21910216 Review.
Juvenile Moyamoya and Craniosynostosis in a Child with Deletion 1p32p31: Expanding the Clinical Spectrum of 1p32p31 Deletion Syndrome and a Review of the Literature.
Prontera P, Rogaia D, Mencarelli A, Ottaviani V, Sallicandro E, Guercini G, Esposito S, Bersano A, Merla G, Stangoni G. Prontera P, et al. Among authors: stangoni g. Int J Mol Sci. 2017 Sep 17;18(9):1998. doi: 10.3390/ijms18091998. Int J Mol Sci. 2017. PMID: 28926972 Free PMC article. Review.
Xq12-q13.3 duplication: evidence of a recurrent syndrome.
Prontera P, Ottaviani V, Isidori I, Stangoni G, Donti E. Prontera P, et al. Among authors: stangoni g. Ann Neurol. 2012 Nov;72(5):821-2; author reply 822-3. doi: 10.1002/ana.23754. Ann Neurol. 2012. PMID: 23280798 No abstract available.
24 results
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