Lv7
4720 积分 2022-02-24 加入
The Inherited Basis of Coronary Artery Disease
17天前
已完结
Canine genome-wide association study identifies DENND1B as an obesity gene in dogs and humans
1个月前
已完结
What are the clues for an inherited metabolic disorder in Reye syndrome? A single Centre study of 58 children
2个月前
已完结
Phosphoserine phosphatase (PSPH) gene mutation in an intellectual disability family from Pakistan
2个月前
已完结
两个营养不良型大疱性表皮松解症家系的基因诊断 Genetic diagnosis in two families with dystrophic epidermolysis bullosa
5个月前
已完结
Correlation between maternal serum biomarkers and the risk of fetal chromosome copy number variants: a single-center retrospective study
5个月前
已完结
Identification of novel biallelic mutations in CFAP53 associated with fetal situs inversus totalis and literature review
5个月前
已完结
Isocucurbitacin B inhibits gliomas through the promotion of anoikis by targeting caveolin 1
5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
5个月前
已完结
Biallelic pathogenic variants in roundabout guidance receptor 1 associate with syndromic congenital anomalies of the kidney and urinary tract
5个月前
已完结
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