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FRA2A is a CGG repeat expansion associated with silencing of AFF3.
PLoS Genet. 2014 Apr 24;10(4):e1004242. doi: 10.1371/journal.pgen.1004242. eCollection 2014 Apr.
PLoS Genet. 2014.
PMID: 24763282
Free PMC article.
A CGG-repeat expansion mutation in ZNF713 causes FRA7A: association with autistic spectrum disorder in two families.
Metsu S, Rainger JK, Debacker K, Bernhard B, Rooms L, Grafodatskaya D, Weksberg R, Fombonne E, Taylor MS, Scherer SW, Kooy RF, FitzPatrick DR.
Metsu S, et al.
Hum Mutat. 2014 Nov;35(11):1295-300. doi: 10.1002/humu.22683.
Hum Mutat. 2014.
PMID: 25196122
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A Survey of Rare Epigenetic Variation in 23,116 Human Genomes Identifies Disease-Relevant Epivariations and CGG Expansions.
Garg P, Jadhav B, Rodriguez OL, Patel N, Martin-Trujillo A, Jain M, Metsu S, Olsen H, Paten B, Ritz B, Kooy RF, Gecz J, Sharp AJ.
Garg P, et al. Among authors: metsu s.
Am J Hum Genet. 2020 Oct 1;107(4):654-669. doi: 10.1016/j.ajhg.2020.08.019. Epub 2020 Sep 15.
Am J Hum Genet. 2020.
PMID: 32937144
Free PMC article.
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Multidisciplinary molecular tumour board: a tool to improve clinical practice and selection accrual for clinical trials in patients with cancer.
Rolfo C, Manca P, Salgado R, Van Dam P, Dendooven A, Ferri Gandia J, Rutten A, Lybaert W, Vermeij J, Gevaert T, Weyn C, Lefebure A, Metsu S, Van Laere S, Peeters M, Pauwels P, Machado Coelho A.
Rolfo C, et al. Among authors: metsu s.
ESMO Open. 2018 Jul 23;3(5):e000398. doi: 10.1136/esmoopen-2018-000398. eCollection 2018.
ESMO Open. 2018.
PMID: 30094075
Free PMC article.
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Rapid clinical mutational testing of KRAS, BRAF and EGFR: a prospective comparative analysis of the Idylla technique with high-throughput next-generation sequencing.
Van Haele M, Vander Borght S, Ceulemans A, Wieërs M, Metsu S, Sagaert X, Weynand B.
Van Haele M, et al. Among authors: metsu s.
J Clin Pathol. 2020 Jan;73(1):35-41. doi: 10.1136/jclinpath-2019-205970. Epub 2019 Jul 11.
J Clin Pathol. 2020.
PMID: 31296605
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