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

Year Number of Results
2005 1
2006 1
2007 4
2008 1
2009 2
2010 1
2011 1
2012 1
2013 2
2014 2
2015 3
2017 1
2018 2
2019 2
2020 3
2021 4
2022 2
2023 0

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24 results

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Page 1
Pathogenic variants in TNRC6B cause a genetic disorder characterised by developmental delay/intellectual disability and a spectrum of neurobehavioural phenotypes including autism and ADHD.
Granadillo JL, P A Stegmann A, Guo H, Xia K, Angle B, Bontempo K, Ranells JD, Newkirk P, Costin C, Viront J, Stumpel CT, Sinnema M, Panis B, Pfundt R, Krapels IPC, Klaassens M, Nicolai J, Li J, Jiang Y, Marco E, Canton A, Latronico AC, Montenegro L, Leheup B, Bonnet C, M Amudhavalli S, Lawson CE, McWalter K, Telegrafi A, Pearson R, Kvarnung M, Wang X, Bi W, Rosenfeld JA, Shinawi M. Granadillo JL, et al. Among authors: klaassens m. J Med Genet. 2020 Oct;57(10):717-724. doi: 10.1136/jmedgenet-2019-106470. Epub 2020 Mar 9. J Med Genet. 2020. PMID: 32152250
Genetic factors in congenital diaphragmatic hernia.
Holder AM, Klaassens M, Tibboel D, de Klein A, Lee B, Scott DA. Holder AM, et al. Among authors: klaassens m. Am J Hum Genet. 2007 May;80(5):825-45. doi: 10.1086/513442. Epub 2007 Apr 4. Am J Hum Genet. 2007. PMID: 17436238 Free PMC article. Review.
Linking animal models to human congenital diaphragmatic hernia.
Beurskens N, Klaassens M, Rottier R, de Klein A, Tibboel D. Beurskens N, et al. Among authors: klaassens m. Birth Defects Res A Clin Mol Teratol. 2007 Aug;79(8):565-72. doi: 10.1002/bdra.20370. Birth Defects Res A Clin Mol Teratol. 2007. PMID: 17469205 Review.
Tibia hemimelia in a patient with CHARGE syndrome: A rare but recurrent phenomenon.
Aukema SM, de Geus CM, Robben SGF, van Kaam KJAF, Staal HM, Witlox AM, de la Haye NAJ, Klaassens M, Coumans A, Stegmann APA, Paley D, Stumpel CTRM. Aukema SM, et al. Among authors: klaassens m. Am J Med Genet A. 2022 Mar;188(3):1000-1004. doi: 10.1002/ajmg.a.62600. Epub 2021 Dec 11. Am J Med Genet A. 2022. PMID: 34894067 No abstract available.
[A boy with digital clubbing].
Van de Ven A, Klaassens M. Van de Ven A, et al. Among authors: klaassens m. Ned Tijdschr Geneeskd. 2017;161:D1807. Ned Tijdschr Geneeskd. 2017. PMID: 29303090 Dutch.
Prenatal detection and outcome of congenital diaphragmatic hernia (CDH) associated with deletion of chromosome 15q26: two patients and review of the literature.
Klaassens M, Galjaard RJ, Scott DA, Brüggenwirth HT, van Opstal D, Fox MV, Higgins RR, Cohen-Overbeek TE, Schoonderwaldt EM, Lee B, Tibboel D, de Klein A. Klaassens M, et al. Am J Med Genet A. 2007 Sep 15;143A(18):2204-12. doi: 10.1002/ajmg.a.31892. Am J Med Genet A. 2007. PMID: 17702015 Review.
24 results