Meizhen Shi
机构：Guangxi Medical University
发表论文 4 篇 · 总被引 19 次 · h-index 2
代表论文
- A homozygous variant in INTS11 links mitosis and neurogenesis defects to a severe neurodevelopmental disorder (2023 · Cell Reports · 被引 15)
- The rare Alus element-mediated chimerism of multiple de novo complex rearrangement sequences in GAN result in giant axonal neuropathy (2019 · Clinica Chimica Acta · 被引 4)
- A hypomorphic SRD5A2 haplotype with a potential founder effect: composed of common variants in individuals with 5α-reductase type 2 deficiency from South China (2026 · Biology of Sex Differences)
- Chromosome Analysis and Postnatal Follow-Up of Fetuses With Abnormal Ultrasound Findings (2021 · Research Square)