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Zhaoli Du

Showing results (11-20 of 14) with videos related to

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Intractable & Rare Diseases Research|November 29, 2023
Identification of novel and <i>de novo GABRB1</i> mutation in Chinese patient with developmental and epileptic encephalopathy 45Shanshan Zhang, Yu Wang, Meilin Liu, et al.
Frontiers in Pediatrics|November 7, 2022
A novel mutation in ryanodine receptor 2 (<i>RYR2</i>) genes at c.12670G>T associated with focal epilepsy in a 3-year-old childJunji Hu, Xueping Gao, Longchang Chen, et al.
Frontiers in Genetics|January 23, 2023
Identification of two rare <i>NPRL3</i> variants in two Chinese families with familial focal epilepsy with variable foci 3: NGS analysis with literature reviewJunji Hu, Xueping Gao, Longchang Chen, et al.
Applied Biochemistry and Biotechnology|May 17, 2022
Identifying Circulating Tumor DNA Mutations Associated with Neoadjuvant Chemotherapy Efficacy in Local Advanced Breast CancerBenjie Wei, Yanhong Shan, Zhaoli Du, et al.
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Showing results (11-20 of 14) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 14 results.
Intractable & Rare Diseases Research|November 29, 2023
Identification of novel and <i>de novo GABRB1</i> mutation in Chinese patient with developmental and epileptic encephalopathy 45Shanshan Zhang, Yu Wang, Meilin Liu, et al.
Frontiers in Pediatrics|November 7, 2022
A novel mutation in ryanodine receptor 2 (<i>RYR2</i>) genes at c.12670G>T associated with focal epilepsy in a 3-year-old childJunji Hu, Xueping Gao, Longchang Chen, et al.
Frontiers in Genetics|January 23, 2023
Identification of two rare <i>NPRL3</i> variants in two Chinese families with familial focal epilepsy with variable foci 3: NGS analysis with literature reviewJunji Hu, Xueping Gao, Longchang Chen, et al.
Applied Biochemistry and Biotechnology|May 17, 2022
Identifying Circulating Tumor DNA Mutations Associated with Neoadjuvant Chemotherapy Efficacy in Local Advanced Breast CancerBenjie Wei, Yanhong Shan, Zhaoli Du, et al.
Pageof 2