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

Year Number of Results
2005 1
2006 2
2007 3
2008 10
2009 4
2010 2
2011 3
2012 6
2013 4
2014 1
2015 2
2017 1
2018 4
2019 6
2020 2
2021 1
2022 1
2023 3
2024 0

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47 results

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Page 1
An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.
Kaminsky EB, Kaul V, Paschall J, Church DM, Bunke B, Kunig D, Moreno-De-Luca D, Moreno-De-Luca A, Mulle JG, Warren ST, Richard G, Compton JG, Fuller AE, Gliem TJ, Huang S, Collinson MN, Beal SJ, Ackley T, Pickering DL, Golden DM, Aston E, Whitby H, Shetty S, Rossi MR, Rudd MK, South ST, Brothman AR, Sanger WG, Iyer RK, Crolla JA, Thorland EC, Aradhya S, Ledbetter DH, Martin CL. Kaminsky EB, et al. Among authors: huang s. Genet Med. 2011 Sep;13(9):777-84. doi: 10.1097/GIM.0b013e31822c79f9. Genet Med. 2011. PMID: 21844811 Free PMC article.
Biomarkers in clinical medicine.
Chen XH, Huang S, Kerr D. Chen XH, et al. Among authors: huang s. IARC Sci Publ. 2011;(163):303-22. IARC Sci Publ. 2011. PMID: 22997869 Review.
Pallister-Killian syndrome: a study of 22 British patients.
Blyth M, Maloney V, Beal S, Collinson M, Huang S, Crolla J, Temple IK, Baralle D. Blyth M, et al. Among authors: huang s. J Med Genet. 2015 Jul;52(7):454-64. doi: 10.1136/jmedgenet-2014-102877. Epub 2015 Apr 17. J Med Genet. 2015. PMID: 25888713
47 results