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

Year Number of Results
2009 1
2010 3
2011 3
2012 3
2013 4
2014 5
2015 4
2016 2
2017 5
2018 1
2019 5
2020 4
2021 2
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35 results
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Page 1
Muscle abnormalities in osteogenesis imperfecta.
Veilleux LN, Trejo P, Rauch F. Veilleux LN, et al. J Musculoskelet Neuronal Interact. 2017 Jun 1;17(2):1-7. J Musculoskelet Neuronal Interact. 2017. PMID: 28574406 Free PMC article. Review.
Identification of genetic variants associated with skeletal muscle function deficit in childhood acute lymphoblastic leukemia survivors.
Nadeau G, Ouimet-Grennan E, Aaron M, Drouin S, Bertout L, Shalmiev A, Beaulieu P, St-Onge P, Veilleux LN, Rauch F, Petrykey K, Laverdière C, Sinnett D, Alos N, Krajinovic M. Nadeau G, et al. Among authors: veilleux ln. Pharmgenomics Pers Med. 2019 Apr 11;12:33-45. doi: 10.2147/PGPM.S192924. eCollection 2019. Pharmgenomics Pers Med. 2019. PMID: 31114288 Free PMC article.
Identification of a single-nucleotide polymorphism within CDH2 gene associated with bone morbidity in childhood acute lymphoblastic leukemia survivors.
Aaron M, Nadeau G, Ouimet-Grennan E, Drouin S, Bertout L, Beaulieu P, St-Onge P, Shalmiev A, Veilleux LN, Rauch F, Petrykey K, Laverdière C, Sinnett D, Alos N, Krajinovic M. Aaron M, et al. Among authors: veilleux ln. Pharmacogenomics. 2019 Apr;20(6):409-420. doi: 10.2217/pgs-2018-0169. Epub 2019 Apr 15. Pharmacogenomics. 2019. PMID: 30983502
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