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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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2021 | 3 |
2022 | 1 |
2024 | 0 |
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Correlation of DUOX2 residual enzymatic activity with phenotype in congenital hypothyroidism caused by biallelic DUOX2 defects.
Clin Genet. 2021 Dec;100(6):713-721. doi: 10.1111/cge.14065. Epub 2021 Sep 29.
Clin Genet. 2021.
PMID: 34564849
The mutation screening in candidate genes related to thyroid dysgenesis by targeted next-generation sequencing panel in the Chinese congenital hypothyroidism.
Zhang RJ, Yang GL, Cheng F, Sun F, Fang Y, Zhang CX, Wang Z, Wu FY, Zhang JX, Zhao SX, Liang J, Song HD.
Zhang RJ, et al.
Clin Endocrinol (Oxf). 2022 Apr;96(4):617-626. doi: 10.1111/cen.14577. Epub 2021 Aug 9.
Clin Endocrinol (Oxf). 2022.
PMID: 34374102
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A five-gene panel refines differential diagnosis of thyroid nodules.
Lu SY, Chen YC, Zhu CF, Chen J, Zhou QY, Zhang MM, Zhang QY, Lu M, Yang L, Wu J, Zhao SX, Song HD, Ye XP.
Lu SY, et al.
J Clin Lab Anal. 2021 Sep;35(9):e23920. doi: 10.1002/jcla.23920. Epub 2021 Jul 28.
J Clin Lab Anal. 2021.
PMID: 34318534
Free PMC article.
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