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BMC Medical Genomics|December 2, 2024
Correlation between rs7041 and rs4588 polymorphisms in vitamin D binding protein gene and COVID-19-related severity and mortalityEman Riad Hamed, Shaymaa Abdelraheem Abdelhady, Shimaa A Al-Touny, et al.
BMC Medical Genomics|November 28, 2024
Protein-losing enteropathy with congenital kidney stones in a 2-month-old boy: a rare case report and literature reviewJiahui Fang, Zhuoheng Li, Lin Zhang, et al.
BMC Medical Genomics|November 29, 2024
A novel frameshift variant in the TMPRSS3 gene causes nonsyndromic hearing loss in a consanguineous familyNahid Rezaie, Saeedeh Sadat Ghazanfari, Seyede Mahsa Mousavikia, et al.
BMC Medical Genomics|February 26, 2025
USP2 reversed cisplatin resistance through p53-mediated ferroptosis in NSCLCYanmei Gong, Ruichao Li, Rui Zhang, et al.
BMC Medical Genomics|February 24, 2025
A novel frameshift variant leads to familial osteopetrosis with variable phenotypes in a Chinese Han consanguineous familyMengxiao Liu, Hao Zheng, Zhixiang Li, et al.
BMC Medical Genomics|November 14, 2025
RNA sequencing provides functional insights and diagnostic resolution in previously unsolved rare disease casesRobert G Lewis, John M O'Shea, Lucilla Pizzo, et al.
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