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Journal of Tropical Pediatrics|August 9, 2024
CTSG polymorphisms in Chinese children with type 1 diabetes mellitusJiaci Li, Mingying Zhang, Shuyue Zhang, et al.
Clinical Genetics|July 30, 2024
Epilepsy due to potential loss of ATP6V1B2 function with mechanistic insight by a Drosophila Vha55 modelWenchao Sheng, Ping Wang, Yingzi Cai, et al.
European Journal of Medical Genetics|July 8, 2019
Mutation spectrum of MMACHC in Chinese pediatric patients with cobalamin C disease: A case series and literature reviewChao Wang, Dong Li, Fengying Cai, et al.
Molecular Genetics & Genomic Medicine|March 22, 2020
Rapid screening of MMACHC gene mutations by high-resolution melting curve analysisChao Wang, Yang Liu, Fengying Cai, et al.
Medicine|January 5, 2019
Clinical and genetic analysis of 7 Chinese patients with β-ureidopropionase deficiencyYulian Fang, Chunquan Cai, Chao Wang, et al.
Molecular Genetics & Genomic Medicine|November 15, 2022
Single nucleotide polymorphisms of PCP pathway related genes participate in the occurrence and development of neural tube defectYan Liu, Liang Dong, Xiufang Zhi, et al.
Frontiers in Microbiology|February 20, 2026
Integrated multi-omics analysis reveals the involvement of the gut-brain axis in children with autismHongping Zhong, Shuyue Zhang, Zichao Mou, et al.
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