Lv31
240 积分 2025-01-23 加入
Alport Syndrome
6天前
待确认
Comparison of Illumina NovaSeq 6000 and GeneMind SURFSeq 5000 platforms for single‐cell spatial transcriptomics of mouse brain and lung
2个月前
已完结
Molecular diagnosis based on comprehensive genetic testing in 800 Chinese families with non-syndromic inherited retinal dystrophies
2个月前
已完结
Identification of CYP4V2 mutation in 36 Chinese families with Bietti crystalline corneoretinal dystrophy
2个月前
已完结
[Clinical, biochemical and gene mutation characteristics of short chain acyl-coenzyme A dehydrogenase deficiency by neonatal screening]
3个月前
已完结
Clinical and Genetic Etiologies of Neonatal Unconjugated Hyperbilirubinemia in the China Neonatal Genomes Project
4个月前
已完结
Nonimmune Hydrops Fetalis
7个月前
已完结
Diamond-Blackfan Anemia
7个月前
已关闭
High Risk Pregnancies in Women with Diamond Blackfan Anaemia: A Survey of 64 Pregnancies from the French and German Registries
7个月前
已完结
Ten novel Diamond–Blackfan anemia mutations and three polymorphisms within the rps19 gene
7个月前
已关闭
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