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

Year Number of Results
1974 2
1975 1
1977 2
1978 1
1980 1
1981 1
1985 2
1986 2
1987 2
1988 1
1989 1
1990 2
1993 1
1994 3
1995 1
1996 1
1997 2
1998 3
1999 2
2000 3
2002 6
2003 4
2004 4
2005 3
2006 3
2007 4
2008 8
2009 3
2011 3
2012 4
2013 4
2014 2
2015 5
2016 3
2017 2
2018 6
2019 4
2020 3
2021 3
2023 2
2024 2

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106 results

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Page 1
[Psychiatry and low intelligence].
van Amelsvoort TAMJ, Zinkstok JR, Vogels A, Wieland J. van Amelsvoort TAMJ, et al. Among authors: vogels a. Tijdschr Psychiatr. 2019;61(11):746-747. Tijdschr Psychiatr. 2019. PMID: 31907882 Free article. Dutch. No abstract available.
Pfeiffer syndrome.
Vogels A, Fryns JP. Vogels A, et al. Orphanet J Rare Dis. 2006 Jun 1;1:19. doi: 10.1186/1750-1172-1-19. Orphanet J Rare Dis. 2006. PMID: 16740155 Free PMC article. Review.
The clinical relevance of intragenic NRXN1 deletions.
Cosemans N, Vandenhove L, Vogels A, Devriendt K, Van Esch H, Van Buggenhout G, Olivié H, de Ravel T, Ortibus E, Legius E, Aerssens P, Breckpot J, R Vermeesch J, Shen S, Fitzgerald J, Gallagher L, Peeters H. Cosemans N, et al. Among authors: vogels a. J Med Genet. 2020 May;57(5):347-355. doi: 10.1136/jmedgenet-2019-106448. Epub 2020 Jan 13. J Med Genet. 2020. PMID: 31932357
Psychotic disorders in Prader-Willi syndrome.
Vogels A, De Hert M, Descheemaeker MJ, Govers V, Devriendt K, Legius E, Prinzie P, Fryns JP. Vogels A, et al. Am J Med Genet A. 2004 Jun 15;127A(3):238-43. doi: 10.1002/ajmg.a.30004. Am J Med Genet A. 2004. PMID: 15150773
8p21.3 deletions are rare causes of non-syndromic autism spectrum disorder.
Cosemans N, Maljaars J, Vogels A, Holvoet M, Devriendt K, Steyaert J, Van Den Bogaert K, Noens I, Peeters H. Cosemans N, et al. Among authors: vogels a. Neurogenetics. 2021 Jul;22(3):207-213. doi: 10.1007/s10048-021-00635-8. Epub 2021 Mar 8. Neurogenetics. 2021. PMID: 33683518
106 results