Lv7
4720 积分 2022-02-24 加入
What are the clues for an inherited metabolic disorder in Reye syndrome? A single Centre study of 58 children
14小时前
已完结
Phosphoserine phosphatase (PSPH) gene mutation in an intellectual disability family from Pakistan
14小时前
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
2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
2个月前
已完结
Identification of novel biallelic mutations in CFAP53 associated with fetal situs inversus totalis and literature review
2个月前
已完结
Isocucurbitacin B inhibits gliomas through the promotion of anoikis by targeting caveolin 1
2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
3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
3个月前
已完结
Chromatin state dynamics confers specific therapeutic strategies in enhancer subtypes of colorectal cancer
3个月前
已完结
AAV9-Mediated Gene Therapy for Infantile-Onset Pompe’s Disease
5个月前
已完结
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