Lv5
1590 积分 2023-08-15 加入
Heterozygosity for a Pathogenic Variant in SLC12A3 That Causes Autosomal Recessive Gitelman Syndrome Is Associated with Lower Serum Potassium
5天前
已完结
Polymorphisms in toll-like receptor 3 and 4 genes as prognostic and outcome biomarkers in melanoma patients
2个月前
已完结
甲状腺肿瘤高通量测序技术基因检测报告模板^(1.0)中国专家共识(2023版)
8个月前
已完结
Dominant-negative variants in CBX1 cause a neurodevelopmental disorder
1年前
已完结
De novo variants in CNOT9 cause a neurodevelopmental disorder with or without epilepsy
1年前
已完结
LHX2 haploinsufficiency causes a variable neurodevelopmental disorder
1年前
已完结
Novel biallelic mutations in PADI6 in patients with early embryonic arrest
1年前
已完结
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