Lv11
40 积分 2025-02-27 加入
Pathogenic Mechanisms in Congenital Afibrinogenemia: A Systematic Review of Genetic Variants
1小时前
待确认
eP326: Genome sequencing reveals BHLHA9 gene duplication as cause of multi-generational split-hand/foot malformation with long bone deficiency
3个月前
已完结
Comprehensive analysis of Chinese patients with non-LPL familial chylomicronemia syndrome: Genetic variants, dietary interventions, and clinical insights
4个月前
已完结
Non-invasive prenatal testing for dominant single-gene disorders using targeted next-generation sequencing
4个月前
已完结
Genetics of glycosylation in mammalian development and disease
4个月前
已完结
A Case Report of 10q24.32 Microduplication Associated with Split Hand/Foot Malformation (SHFM) in Prenatal Diagnosis
5个月前
已完结
Distal limb deficiencies, micrognathia syndrome, and syndromic forms of split hand foot malformation (SHFM) are caused by chromosome 10q genomic rearrangements
5个月前
已完结
Methods of Detection and Mechanisms of Origin of Complex Structural Genome Variations
5个月前
已完结
Uterus‐Mimetic Extracellular Microenvironment for Engineering Female Reproductive System
6个月前
已完结
Multiplex generation and single cell analysis of structural variants in a mammalian genome
6个月前
已完结
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