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Wenting Tang

Showing results (31-40 of 110) with videos related to

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American Journal of Medical Genetics. Part A|April 9, 2024
Identification of a novel phenotype of external ear deformity related to Coffin-Siris syndrome-9 and literature reviewRuohao Wu, Wenting Tang, Pinggan Li, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|September 14, 2019
[Analysis of HEXB gene mutations in an infant with Sandhoff disease]Ruohao Wu, Wenting Tang, Kunyin Qiu, et al.
Zhongguo Zhong Yao Za Zhi = Zhongguo Zhongyao Zazhi = China Journal of Chinese Materia Medica|October 25, 2011
[Correlation between environmental factors and liposoluble and hydrophilic constituents of Polygalae Radix]Minfeng Fang, Yang Wu, Ming Yue, et al.
International Journal of Clinical and Experimental Pathology|January 15, 2020
EBV-associated myoid tumor with lipoblast-like cells in a patient with normal immunityRuohao Wu, Wenting Tang, Danxia Tang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|September 14, 2020
[Identification of a novel frameshift variant in the SRCAP gene of a child with Floating-Harbor syndrome]Ruohao Wu, Wenting Tang, Kunyin Qiu, et al.
BMC Cancer|April 4, 2023
Clinical significance of nonerythrocytic spectrin Beta 1 (SPTBN1) in human kidney renal clear cell carcinoma and uveal melanoma: a study based on Pan-Cancer AnalysisWenting Tang, Qiong Shao, Zhanwen He, et al.
Experimental Biology and Medicine (Maywood, N.J.)|March 21, 2023
Stattic alleviates pulmonary fibrosis in a mouse model of rheumatoid arthritis-relevant interstitial lung diseaseLihu Xie, Youyou Li, Wenting Tang, et al.
Frontiers in Neurology|October 23, 2025
Predicting the diagnostic efficacy of trio-based whole exome sequencing in children with low-function autism spectrum disorders: a multicenter studyRuohao Wu, Xiangyang Luo, Zhanwen He, et al.
BMC Pediatrics|October 6, 2025
Multiple phenotypic traits including developmental impairment in a Chinese family with infantile convulsion and choreoathetosis syndrome: a case study expanding the clinical spectrum of prrt2-related syndromeRuohao Wu, Xiaojuan Li, Zhanwen He, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 8, 2021
[Clinical and genetic analysis of a family with autosomal dominant-familial Mediterranean fever]Dongfang Li, Wenting Tang, Kunyin Qiu, et al.
Pageof 11

Showing results (31-40 of 110) with videos related to

Sort By:
Pageof 11
American Journal of Medical Genetics. Part A|April 9, 2024
Identification of a novel phenotype of external ear deformity related to Coffin-Siris syndrome-9 and literature reviewRuohao Wu, Wenting Tang, Pinggan Li, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|September 14, 2019
[Analysis of HEXB gene mutations in an infant with Sandhoff disease]Ruohao Wu, Wenting Tang, Kunyin Qiu, et al.
Zhongguo Zhong Yao Za Zhi = Zhongguo Zhongyao Zazhi = China Journal of Chinese Materia Medica|October 25, 2011
[Correlation between environmental factors and liposoluble and hydrophilic constituents of Polygalae Radix]Minfeng Fang, Yang Wu, Ming Yue, et al.
International Journal of Clinical and Experimental Pathology|January 15, 2020
EBV-associated myoid tumor with lipoblast-like cells in a patient with normal immunityRuohao Wu, Wenting Tang, Danxia Tang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|September 14, 2020
[Identification of a novel frameshift variant in the SRCAP gene of a child with Floating-Harbor syndrome]Ruohao Wu, Wenting Tang, Kunyin Qiu, et al.
BMC Cancer|April 4, 2023
Clinical significance of nonerythrocytic spectrin Beta 1 (SPTBN1) in human kidney renal clear cell carcinoma and uveal melanoma: a study based on Pan-Cancer AnalysisWenting Tang, Qiong Shao, Zhanwen He, et al.
Experimental Biology and Medicine (Maywood, N.J.)|March 21, 2023
Stattic alleviates pulmonary fibrosis in a mouse model of rheumatoid arthritis-relevant interstitial lung diseaseLihu Xie, Youyou Li, Wenting Tang, et al.
Frontiers in Neurology|October 23, 2025
Predicting the diagnostic efficacy of trio-based whole exome sequencing in children with low-function autism spectrum disorders: a multicenter studyRuohao Wu, Xiangyang Luo, Zhanwen He, et al.
BMC Pediatrics|October 6, 2025
Multiple phenotypic traits including developmental impairment in a Chinese family with infantile convulsion and choreoathetosis syndrome: a case study expanding the clinical spectrum of prrt2-related syndromeRuohao Wu, Xiaojuan Li, Zhanwen He, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 8, 2021
[Clinical and genetic analysis of a family with autosomal dominant-familial Mediterranean fever]Dongfang Li, Wenting Tang, Kunyin Qiu, et al.
Pageof 11