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Yilun Tao

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

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Frontiers in Genetics|September 11, 2023
A <i>GATA3</i> gene mutation that causes incorrect splicing and HDR syndrome: a case study and literature reviewYilun Tao, Lin Yang, Dong Han, et al.
Frontiers in Genetics|May 7, 2025
Novel <i>ACAD8</i> variants identified in Isobutyryl-CoA dehydrogenase deficiency: challenges in phenotypic variability and managementYilun Tao, Dong Han, Jianfang Li, et al.
Molecular Genetics & Genomic Medicine|October 11, 2023
Novel HPD mutation p.A244V compound with p.T219M causing tyrosinemia type III in a Chinese girl and review of the genotype-phenotype spectrumDong Han, Lihong Wang, Chen Zhao, et al.
Frontiers in Genetics|July 8, 2025
Uncovering genetic contributors to developmental delay and intellectual disability: a focus on CNVs in pediatric patientsYilun Tao, Hongzhi Guo, Dong Han, et al.
Pageof 2

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.
Frontiers in Genetics|September 11, 2023
A <i>GATA3</i> gene mutation that causes incorrect splicing and HDR syndrome: a case study and literature reviewYilun Tao, Lin Yang, Dong Han, et al.
Frontiers in Genetics|May 7, 2025
Novel <i>ACAD8</i> variants identified in Isobutyryl-CoA dehydrogenase deficiency: challenges in phenotypic variability and managementYilun Tao, Dong Han, Jianfang Li, et al.
Molecular Genetics & Genomic Medicine|October 11, 2023
Novel HPD mutation p.A244V compound with p.T219M causing tyrosinemia type III in a Chinese girl and review of the genotype-phenotype spectrumDong Han, Lihong Wang, Chen Zhao, et al.
Frontiers in Genetics|July 8, 2025
Uncovering genetic contributors to developmental delay and intellectual disability: a focus on CNVs in pediatric patientsYilun Tao, Hongzhi Guo, Dong Han, et al.
Pageof 2