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Na Lin

Showing results (511-520 of 974) with videos related to

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Medicine|May 20, 2021
Diagnostic accuracy and value of chromosomal microarray analysis for chromosomal abnormalities in prenatal detection: A prospective clinical studyHailong Huang, Yan Wang, Min Zhang, et al.
BMC Medical Genomics|December 21, 2022
Clinical findings and genetic analysis of patients with copy number variants involving 17p13.3 using a single nucleotide polymorphism array: a single-center experienceBin Liang, Donghong Yu, Wantong Zhao, et al.
Inorganic Chemistry|October 2, 2013
Ba13Si6Sn8As22: a quaternary Zintl phase containing adamantane-like [Si4As10] clustersXiao-Cun Liu, Na Lin, Jian Wang, et al.
Frontiers in Pediatrics|July 5, 2022
Chromosomal Abnormalities and Pregnancy Outcomes for Fetuses With Gastrointestinal Tract ObstructionsXiaoqing Wu, Linjuan Su, Qingmei Shen, et al.
Journal of Applied Microbiology|January 11, 2024
Antifungal mechanism of rose, mustard, and their blended essential oils against Cladosporium allicinum isolated from Xinjiang naan and its storage applicationYu-Han Yuan, Xiang-Na Lin, Xiao-Mei Xu, et al.
Food Research International (Ottawa, Ont.)|May 17, 2024
Metabolomics analysis of physicochemical properties associated with freshness degradation in frozen Antarctic krill (Euphausia superba)Ling Ni, Chaojun Jiang, Quanyou Guo, et al.
Molecular Biology Reports|September 16, 2020
Prenatal diagnosis of 22q11.2 copy number abnormalities in fetuses via single nucleotide polymorphism arrayMeiying Cai, Na Lin, Linjuan Su, et al.
International Journal of Clinical and Experimental Pathology|January 15, 2020
Identification of a novel pre-terminating mutation in human HBB gene as a cause of β<sup>0</sup>-thalassemia phenotypeLiangpu Xu, Meihuan Chen, Hailong Huang, et al.
International Journal of Clinical and Experimental Pathology|January 18, 2020
A rare α-thalassemia deletion, -α<sup>27.6</sup>, is identified from three Chinese families in Fujian provinceHailong Huang, Meihuan Chen, Xuemei Chen, et al.
Oncotarget|July 8, 2016
Thyroid hormone synthesis: a potential target of a Chinese herbal formula Haizao Yuhu Decoction acting on iodine-deficient goiterYanqiong Zhang, Yuting Li, Xia Mao, et al.
Pageof 98

Showing results (511-520 of 974) with videos related to

Sort By:
Pageof 98
Medicine|May 20, 2021
Diagnostic accuracy and value of chromosomal microarray analysis for chromosomal abnormalities in prenatal detection: A prospective clinical studyHailong Huang, Yan Wang, Min Zhang, et al.
BMC Medical Genomics|December 21, 2022
Clinical findings and genetic analysis of patients with copy number variants involving 17p13.3 using a single nucleotide polymorphism array: a single-center experienceBin Liang, Donghong Yu, Wantong Zhao, et al.
Inorganic Chemistry|October 2, 2013
Ba13Si6Sn8As22: a quaternary Zintl phase containing adamantane-like [Si4As10] clustersXiao-Cun Liu, Na Lin, Jian Wang, et al.
Frontiers in Pediatrics|July 5, 2022
Chromosomal Abnormalities and Pregnancy Outcomes for Fetuses With Gastrointestinal Tract ObstructionsXiaoqing Wu, Linjuan Su, Qingmei Shen, et al.
Journal of Applied Microbiology|January 11, 2024
Antifungal mechanism of rose, mustard, and their blended essential oils against Cladosporium allicinum isolated from Xinjiang naan and its storage applicationYu-Han Yuan, Xiang-Na Lin, Xiao-Mei Xu, et al.
Food Research International (Ottawa, Ont.)|May 17, 2024
Metabolomics analysis of physicochemical properties associated with freshness degradation in frozen Antarctic krill (Euphausia superba)Ling Ni, Chaojun Jiang, Quanyou Guo, et al.
Molecular Biology Reports|September 16, 2020
Prenatal diagnosis of 22q11.2 copy number abnormalities in fetuses via single nucleotide polymorphism arrayMeiying Cai, Na Lin, Linjuan Su, et al.
International Journal of Clinical and Experimental Pathology|January 15, 2020
Identification of a novel pre-terminating mutation in human HBB gene as a cause of β<sup>0</sup>-thalassemia phenotypeLiangpu Xu, Meihuan Chen, Hailong Huang, et al.
International Journal of Clinical and Experimental Pathology|January 18, 2020
A rare α-thalassemia deletion, -α<sup>27.6</sup>, is identified from three Chinese families in Fujian provinceHailong Huang, Meihuan Chen, Xuemei Chen, et al.
Oncotarget|July 8, 2016
Thyroid hormone synthesis: a potential target of a Chinese herbal formula Haizao Yuhu Decoction acting on iodine-deficient goiterYanqiong Zhang, Yuting Li, Xia Mao, et al.
Pageof 98