Lv1
38 积分 2023-03-22 加入
Phenotypic variability in distal acidification defects associated with WDR72 mutations
3个月前
已完结
Distal renal tubular acidosis caused by tryptophan‐aspartate repeat domain 72 (WDR72) mutations
3个月前
已完结
SON基因新发移码突变致ZTTK综合征1例的临床特征及遗传学分析
5个月前
已完结
Clinical characteristics and genetic profile of children with WDR72-associated distal renal tubular acidosis: a nationwide experience
5个月前
已完结
[Genomic and post-genomic era genetic research and clinical practice of hereditary kidney diseases]
5个月前
已完结
How can clinicians accurately diagnose hereditary kidney diseases in the genomic era
5个月前
已完结
A kidney-disease gene panel allows a comprehensive genetic diagnosis of cystic and glomerular inherited kidney diseases
6个月前
已完结
Genetic spectrum of renal disease for 1001 Chinese children based on a multicenter registration system
6个月前
已完结
Artificial Intelligence in the Genetic Diagnosis of Rare Disease
6个月前
已完结
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