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

Year Number of Results
2006 1
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2008 1
2009 1
2010 3
2011 5
2012 8
2013 5
2014 3
2015 3
2016 4
2017 6
2018 8
2019 3
2020 3
2021 11
2022 10
2023 4
2024 1

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72 results

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Page 1
Genetics of Hirschsprung's disease.
Tang CS, Karim A, Zhong Y, Chung PH, Tam PK. Tang CS, et al. Pediatr Surg Int. 2023 Feb 7;39(1):104. doi: 10.1007/s00383-022-05358-x. Pediatr Surg Int. 2023. PMID: 36749416 Review.
NGS4THAL, a One-Stop Molecular Diagnosis and Carrier Screening Tool for Thalassemia and Other Hemoglobinopathies by Next-Generation Sequencing.
Cao Y, Ha SY, So CC, Tong MT, Tang CS, Zhang H, Liang R, Yang J, Chung BH, Chan GC, Lau YL, Garcia-Barcelo MM, Ma ES, Sucharitchan P, Hirankarn N, Yang W. Cao Y, et al. Among authors: tang cs. J Mol Diagn. 2022 Oct;24(10):1089-1099. doi: 10.1016/j.jmoldx.2022.06.006. Epub 2022 Jul 19. J Mol Diagn. 2022. PMID: 35868510 Free article.
Differential vulnerability of hippocampal CA3-CA1 synapses to Aβ.
Shipton OA, Tang CS, Paulsen O, Vargas-Caballero M. Shipton OA, et al. Among authors: tang cs. Acta Neuropathol Commun. 2022 Apr 4;10(1):45. doi: 10.1186/s40478-022-01350-7. Acta Neuropathol Commun. 2022. PMID: 35379353 Free PMC article.
Comprehensive analysis of recessive carrier status using exome and genome sequencing data in 1543 Southern Chinese.
Chau JFT, Yu MHC, Chui MMC, Yeung CCW, Kwok AWC, Zhuang X, Lee R, Fung JLF, Lee M, Mak CCY, Ng NYT, Chung CCY, Chan MCY, Tsang MHY, Chan JCK, Chan KYK, Kan ASY, Chung PHY, Yang W, Lee SL, Chan GCF, Tam PKH, Lau YL, Yeung KS, Chung BHY, Tang CSM. Chau JFT, et al. Among authors: tang csm. NPJ Genom Med. 2022 Mar 21;7(1):23. doi: 10.1038/s41525-022-00287-z. NPJ Genom Med. 2022. PMID: 35314707 Free PMC article.
72 results