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

Year Number of Results
2005 4
2007 2
2008 2
2011 3
2012 3
2013 4
2014 3
2015 1
2016 1
2017 8
2018 4
2019 10
2020 10
2021 11
2022 9
2023 12
2024 1

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79 results

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Page 1
Application of next generation sequencing in the screening of monogenic diseases in China, 2021: a consensus among Chinese newborn screening experts.
Tong F, Wang J, Xiao R, Wu BB, Zou CC, Wu DW, Wang H, Zou H, Han LS, Yang L, Zou L, Hei MY, Yang RL, Yuan TM, Wen W, Huang XW, Gu XF, Yang YL, Huang YL, Zhang YJ, Yu YG, Xu ZF, Zhou WH, Zhao ZY. Tong F, et al. World J Pediatr. 2022 Apr;18(4):235-242. doi: 10.1007/s12519-022-00522-8. Epub 2022 Mar 15. World J Pediatr. 2022. PMID: 35292922 No abstract available.
ATAD3A gene variations in a family with Harel-Yoon syndrome.
Zheng Y, Yu X, Zhang T, Hu L, Zhou D, Huang X. Zheng Y, et al. Among authors: huang x. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2023 Dec 7;52(6):738-743. doi: 10.3724/zdxbyxb-2023-0421. Zhejiang Da Xue Xue Bao Yi Xue Ban. 2023. PMID: 38105692 Free PMC article. Chinese, English.
[Expert consensus for the diagnosis and treatment of glutaricacidemia type 1].
Endocrinology, Genetics and Metabolism Group,Pediatric Branch of Chinese Medical Association; Neonatal Screening Group, Specialist Committee for Prevention and Control of Birth Defects Chinese Association of Preventive Medicine; Prevention and Control Committee of Birth Defects, Pediatric Branch of Chinese Medical Association; Han L, Yang Y, Yang R, Chen R, Huang X. Endocrinology, Genetics and Metabolism Group,Pediatric Branch of Chinese Medical Association, et al. Among authors: huang x. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021 Jan 10;38(1):1-6. doi: 10.3760/cma.j.cn511374-20200705-00495. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2021. PMID: 33423247 Chinese.
79 results