Lv61
1650 积分 2023-08-15 加入
Microbial Interactions Induce the Mutational Signature of Mismatch Repair Deficiency in Colorectal Cancer and Associated with EPPK1 Mutations
5小时前
已关闭
The transcription factor Zeb1 controls homeostasis and function of type 1 conventional dendritic cells
5小时前
已完结
Long-Read Sequencing Solves Complex Structure of CYP21A2 in a Large 21-Hydroxylase Deficiency Cohort
7个月前
已完结
Heterozygosity for a Pathogenic Variant in SLC12A3 That Causes Autosomal Recessive Gitelman Syndrome Is Associated with Lower Serum Potassium
9个月前
已完结
Polymorphisms in toll-like receptor 3 and 4 genes as prognostic and outcome biomarkers in melanoma patients
11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)
1年前
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
皖公网安备34019202002308
