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

Year Number of Results
1996 1
1997 2
1999 1
2000 1
2001 2
2002 2
2003 2
2004 3
2005 2
2006 3
2007 2
2008 4
2009 3
2010 7
2011 6
2012 1
2013 3
2014 6
2015 4
2016 5
2017 3
2018 8
2019 10
2020 5
2021 5
2022 3
2023 3
2024 3

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PubMed for id: 4212

87 results

Results by year

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Page 1
Intellectual disability associated with craniofacial dysmorphism, cleft palate, and congenital heart defect due to a de novo MEIS2 mutation: A clinical longitudinal study.
Gangfuß A, Yigit G, Altmüller J, Nürnberg P, Czeschik JC, Wollnik B, Bögershausen N, Burfeind P, Wieczorek D, Kaiser F, Roos A, Kölbel H, Schara-Schmidt U, Kuechler A. Gangfuß A, et al. Am J Med Genet A. 2021 Apr;185(4):1216-1221. doi: 10.1002/ajmg.a.62070. Epub 2021 Jan 11. Am J Med Genet A. 2021. PMID: 33427397
Epigenetic silencing of MEIS2 in prostate cancer recurrence.
Nørgaard M, Haldrup C, Bjerre MT, Høyer S, Ulhøi B, Borre M, Sørensen KD. Nørgaard M, et al. Clin Epigenetics. 2019 Oct 22;11(1):147. doi: 10.1186/s13148-019-0742-x. Clin Epigenetics. 2019. PMID: 31640805 Free PMC article.
MEIS2 promotes cell migration and invasion in colorectal cancer.
Wan Z, Chai R, Yuan H, Chen B, Dong Q, Zheng B, Mou X, Pan W, Tu Y, Yang Q, Tu S, Hu X. Wan Z, et al. Oncol Rep. 2019 Jul;42(1):213-223. doi: 10.3892/or.2019.7161. Epub 2019 May 15. Oncol Rep. 2019. PMID: 31115559 Free PMC article.
De novo missense variants in MEIS2 recapitulate the microdeletion phenotype of cardiac and palate abnormalities, developmental delay, intellectual disability and dysmorphic features.
Douglas G, Cho MT, Telegrafi A, Winter S, Carmichael J, Zackai EH, Deardorff MA, Harr M, Williams L, Psychogios A, Erwin AL, Grebe T, Retterer K, Juusola J. Douglas G, et al. Am J Med Genet A. 2018 Sep;176(9):1845-1851. doi: 10.1002/ajmg.a.40368. Epub 2018 Jul 28. Am J Med Genet A. 2018. PMID: 30055086
87 results