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Zhonghua Yi Xue Za Zhi|March 28, 2019
[Molecular and clinical study on homozygous or heterozygous large deletion of <i>CYP21A2</i> gene in 21-OHD patients]Y J Gao, B Q Yu, L Lu, et al.
Zhonghua Yi Xue Za Zhi|December 26, 2019
[Analysis of copy number variation of <i>CYP21A2</i> gene and the type of <i>CYP21A1P</i>/<i>CYP21A2</i> fused gene in patients with 21-hydroxylase deficiency]Y J Gao, B Q Yu, L Lu, et al.
Zhonghua Yi Xue Za Zhi|March 13, 2020
[Detection of CYP21A2 gene mutations and the differences in the levels of hormones in patients with 21-hydroxylase deficiency]Y J Gao, B Q Yu, L Lu, et al.
Zhonghua Jie He He Hu Xi Za Zhi = Zhonghua Jiehe He Huxi Zazhi = Chinese Journal of Tuberculosis and Respiratory Diseases|June 10, 2025
[Dyskeratosis congenita combined with myeloproliferative disorder and trilineage cytopenia]Y L Peng, X T Qian, Y Q Tian, et al.
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|September 29, 2021
[Clinical analysis of 60 children with anaplastic large cell lymphoma in a single center]M Wang, Q Mi, Q Yuan, et al.
European Review for Medical and Pharmacological Sciences|March 4, 2021
Abnormalities of the default-mode network homogeneity and executive dysfunction in people with first-episode, treatment-naive left temporal lobe epilepsyY-J Gao, X Wang, P-G Xiong, et al.
Zhonghua Yi Xue Za Zhi|September 26, 2022
[Prognostic value of translocation t(11;14) in primary light-chain amyloidosis treated with bortezomib-based regimen]Y J Gao, K N Shen, J Feng, et al.
Genetics and Molecular Research : GMR|October 28, 2015
¹H-MRS before and after resuscitation following selective cerebral ultra-profound hypothermic blood flow occlusion in monkeysX-Q Niu, X-X Zhao, B-C Li, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 19, 1997
Importance of epistasis as the genetic basis of heterosis in an elite rice hybridS B Yu, J X Li, C G Xu, et al.
Zhonghua Xin Xue Guan Bing Za Zhi|September 15, 2025
[An exploratory study on new indicators of AVS in the typing diagnosis of primary aldosteronism]Z W Li, Y Wang, Y J Gao, et al.
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