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Yi Chuan = Hereditas|February 8, 2007
[FUT1 gene polymorphism and its association with litter size in pigs]Yin-Hong Zhang, Zhong-Xiao Zhou, Guo-Qing Cao
Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy|September 4, 2022
Highly selective and multicolor ultrasensitive assay of dipicolinic acid: The integration of terbium(III) and gold nanoclusterNing Bi, Yin-Hong Zhang, Mei-Hua Hu, et al.
Immunobiology|March 9, 2025
Harnessing miR-16-5p-Loaded Exosomes from Adipose-Derived Stem Cells to Restore Immune Homeostasis in SLE PatientsYin-Hong Zhang, Juan Chen, Wen-Fei Mao, et al.
Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics|January 25, 2015
[Analysis of neonatal screening results for congenital hypothyroidism in parts of Yunnan Province, China]Yin-Hong Zhang, Li Li, Hong Chen, et al.
Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics|December 16, 2021
Follow-up study of preterm infants with thyroid dysfunction after medicationFeng-Chao Li, Jian-Ying Duan, Yin-Hong Zhang, et al.
Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics|December 16, 2025
[Clinical and genetic characteristics of 14 children with sodium taurocholate co-transporting polypeptide deficiency]Rui-Xue Ma, Wen-Hai Luo, Yi-Lin Dai, et al.
Zhonghua Fu Chan Ke Za Zhi|March 30, 2012
[A study on gene mutation spectrums of α- and β-thalassemias in populations of Yunnan Province and the prenatal gene diagnosis]Bao-sheng Zhu, Jing He, Jie Zhang, et al.
Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics|July 13, 2017
[Analysis of treatment efficacy for congenital hypothyroidism in some regions of Yunnan Province, China]Jing-Hui Yang, Jing-Hui Zhang, Yin-Hong Zhang, et al.
Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics|June 30, 2025
[Genetic screening and follow-up results in 3 001 newborns in the Yunnan region]Ao-Yu Li, Bao-Sheng Zhu, Jin-Man Zhang, et al.
Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics|March 26, 2019
[Association of copy number of SMN1 and SMN2 with clinical phenotypes in children with spinal muscular atrophy]Yin-Hong Zhang, Yun-Qian Zhang, Bao-Sheng Zhu, et al.
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