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Results by year

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

Year Number of Results
1971 1
1977 1
1978 1
1987 1
1991 3
1992 1
1994 1
1995 1
1996 2
1997 1
1998 2
1999 2
2000 3
2001 2
2002 4
2003 2
2004 1
2005 2
2006 3
2007 9
2009 4
2010 3
2011 7
2012 8
2013 8
2014 6
2015 8
2016 5
2017 1
2018 4
2020 4
2021 3
2022 5
2023 1
2024 0

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PubMed for id: 341506

102 results

Results by year

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Page 1
Case report of a novel phenotype in 18q deletion syndrome.
Bohîlţea RE, Cîrstoiu MM, Nedelea FM, Turcan N, Georgescu TA, Munteanu O, Baroş A, Istrate-Ofiţeru AM, Berceanu C. Bohîlţea RE, et al. Rom J Morphol Embryol. 2020 Jul-Sep;61(3):905-910. doi: 10.47162/RJME.61.3.29. Rom J Morphol Embryol. 2020. PMID: 33817732 Free PMC article.
Clinical and molecular description of 19 patients with GATAD2B-Associated Neurodevelopmental Disorder (GAND).
Vera G, Sorlin A, Delplancq G, Lecoquierre F, Brasseur-Daudruy M, Petit F, Smol T, Ziegler A, Bonneau D, Colin E, Mercier S, Cogné B, Bézieau S, Edery P, Lesca G, Chatron N, Sabatier I, Duban-Bedu B, Colson C, Piton A, Durand B, Capri Y, Perrin L, Wiesener A, Zweier C, Maroofian R, Carroll CJ, Galehdari H, Mazaheri N, Callewaert B, Giulianno F, Zaafrane-Khachnaoui K, Buchert-Lo R, Haack T, Magg J, Rieß A, Blandfort M, Waldmüller S, Horber V, Leonardi E, Polli R, Turolla L, Murgia A, Frebourg T, Lebre AS, Nicolas G, Saugier-Veber P, Guerrot AM. Vera G, et al. Eur J Med Genet. 2020 Oct;63(10):104004. doi: 10.1016/j.ejmg.2020.104004. Epub 2020 Jul 17. Eur J Med Genet. 2020. PMID: 32688057
Characterization of a recurrent 15q24 microdeletion syndrome.
Sharp AJ, Selzer RR, Veltman JA, Gimelli S, Gimelli G, Striano P, Coppola A, Regan R, Price SM, Knoers NV, Eis PS, Brunner HG, Hennekam RC, Knight SJ, de Vries BB, Zuffardi O, Eichler EE. Sharp AJ, et al. Hum Mol Genet. 2007 Mar 1;16(5):567-72. doi: 10.1093/hmg/ddm016. Epub 2007 Mar 14. Hum Mol Genet. 2007. PMID: 17360722
Deletion short arm 18 and Silver-Russell syndrome.
Christensen MF, Nielsen J. Christensen MF, et al. Acta Paediatr Scand. 1978 Jan;67(1):101-3. doi: 10.1111/j.1651-2227.1978.tb16284.x. Acta Paediatr Scand. 1978. PMID: 626060
102 results