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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
1975 5
1976 2
1977 6
1978 3
1979 4
1980 7
1981 7
1982 11
1983 9
1984 8
1985 13
1986 13
1987 15
1988 11
1989 12
1990 13
1991 8
1992 18
1993 20
1994 21
1995 21
1996 23
1997 23
1998 20
1999 25
2000 42
2001 38
2002 21
2003 25
2004 22
2005 29
2006 31
2007 34
2008 30
2009 30
2010 47
2011 35
2012 31
2013 39
2014 38
2015 37
2016 29
2017 22
2018 30
2019 31
2020 28
2021 32
2022 31
2023 21
2024 5

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PubMed for id: 376232

992 results

Results by year

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Page 1
TCEAL1 loss-of-function results in an X-linked dominant neurodevelopmental syndrome and drives the neurological disease trait in Xq22.2 deletions.
Hijazi H, Reis LM, Pehlivan D, Bernstein JA, Muriello M, Syverson E, Bonner D, Estiar MA, Gan-Or Z, Rouleau GA, Lyulcheva E, Greenhalgh L, Tessarech M, Colin E, Guichet A, Bonneau D, van Jaarsveld RH, Lachmeijer AMA, Ruaud L, Levy J, Tabet AC, Ploski R, Rydzanicz M, Kępczyński Ł, Połatyńska K, Li Y, Fatih JM, Marafi D, Rosenfeld JA, Coban-Akdemir Z, Bi W, Gibbs RA, Hobson GM, Hunter JV, Carvalho CMB, Posey JE, Semina EV, Lupski JR. Hijazi H, et al. Am J Hum Genet. 2022 Dec 1;109(12):2270-2282. doi: 10.1016/j.ajhg.2022.10.007. Epub 2022 Nov 10. Am J Hum Genet. 2022. PMID: 36368327 Free PMC article.
992 results