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

Year Number of Results
2002 2
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2010 5
2011 5
2012 5
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Page 1
Whole-Exome Sequencing in Congenital Hypothyroidism Due to Thyroid Dysgenesis.
Larrivée-Vanier S, Jean-Louis M, Magne F, Bui H, Rouleau GA, Spiegelman D, Samuels ME, Kibar Z, Van Vliet G, Deladoëy J. Larrivée-Vanier S, et al. Among authors: samuels me. Thyroid. 2022 May;32(5):486-495. doi: 10.1089/thy.2021.0597. Epub 2022 Apr 25. Thyroid. 2022. PMID: 35272499 Free PMC article.
Genetics of the patella.
Samuels ME, Campeau PM. Samuels ME, et al. Eur J Hum Genet. 2019 May;27(5):671-680. doi: 10.1038/s41431-018-0329-6. Epub 2019 Jan 21. Eur J Hum Genet. 2019. PMID: 30664715 Free PMC article. Review.
Evolution of the patellar sesamoid bone in mammals.
Samuels ME, Regnault S, Hutchinson JR. Samuels ME, et al. PeerJ. 2017 Mar 21;5:e3103. doi: 10.7717/peerj.3103. eCollection 2017. PeerJ. 2017. PMID: 28344905 Free PMC article.
Family Based Whole Exome Sequencing Reveals the Multifaceted Role of Notch Signaling in Congenital Heart Disease.
Preuss C, Capredon M, Wünnemann F, Chetaille P, Prince A, Godard B, Leclerc S, Sobreira N, Ling H, Awadalla P, Thibeault M, Khairy P; MIBAVA Leducq consortium; Samuels ME, Andelfinger G. Preuss C, et al. Among authors: samuels me. PLoS Genet. 2016 Oct 19;12(10):e1006335. doi: 10.1371/journal.pgen.1006335. eCollection 2016 Oct. PLoS Genet. 2016. PMID: 27760138 Free PMC article.
56 results