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

Year Number of Results
1979 1
1982 1
1984 1
1985 1
1991 1
1992 2
1997 1
1998 1
1999 1
2002 1
2003 1
2006 1
2007 1
2010 4
2011 1
2012 1
2013 4
2014 5
2015 6
2016 8
2017 9
2018 5
2019 5
2020 4
2021 3
2022 4
2023 1
2024 0

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Similar articles for PMID: 30179896

61 results

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Page 1
UBE2A-related X-linked intellectual disability.
Stevenson RE, Chudley AE, Srivastava AK, Rodriguez J, Friez MJ, Schwartz CE. Stevenson RE, et al. Clin Dysmorphol. 2019 Jan;28(1):1-6. doi: 10.1097/MCD.0000000000000242. Clin Dysmorphol. 2019. PMID: 30179896 Free PMC article.
Refinement of the clinical and mutational spectrum of UBE2A deficiency syndrome.
Cordeddu V, Macke EL, Radio FC, Lo Cicero S, Pantaleoni F, Tatti M, Bellacchio E, Ciolfi A, Agolini E, Bruselles A, Brunetti-Pierri N, Suri M, Josephs KS, McEntagart M, Lanpher B, Nickels KC, Haworth A, Reed L, Cappuccio G, Mammi I, Tarnowski JM, Novelli A; Deciphering Developmental Disorders Study; Melis D, Callewaert B, Dallapiccola B, Klee E, Tartaglia M. Cordeddu V, et al. Clin Genet. 2020 Aug;98(2):172-178. doi: 10.1111/cge.13775. Epub 2020 Jun 3. Clin Genet. 2020. PMID: 32415735
Mechanistic insights revealed by a UBE2A mutation linked to intellectual disability.
de Oliveira JF, do Prado PFV, da Costa SS, Sforça ML, Canateli C, Ranzani AT, Maschietto M, de Oliveira PSL, Otto PA, Klevit RE, Krepischi ACV, Rosenberg C, Franchini KG. de Oliveira JF, et al. Nat Chem Biol. 2019 Jan;15(1):62-70. doi: 10.1038/s41589-018-0177-2. Epub 2018 Dec 10. Nat Chem Biol. 2019. PMID: 30531907 Free PMC article.
61 results