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Human Genomics|April 24, 2026
Multigenerational evidence of X-linked adrenal hypoplasia congenita due to a novel NR0B1 frameshiftLang Tian, Jie Mei, Xi Zheng, et al.Human Genomics|April 9, 2026
Integrated multiomics profiling of amniotic fluid exosomes reveals dysregulated lipid and protein signatures in fetal 22q11.2 deletion syndromeHai Xiao, Tao Li, Mengting Zhang, et al.Human Genomics|May 8, 2026
Machine learning-based transcriptomic analysis of differentially expressed genes in the epithelium and stroma of keratoconusKaiyue Du, Rongmei Peng, Gege Xiao, et al.Pageof 112