Lv4
712 积分 2022-11-13 加入
Open-Label Treatment Trial of Lithium to Target the Underlying Defect in Fragile X Syndrome
6天前
已完结
Lithium Formulations in Clinical Practice
6天前
已完结
Later onset of Childhood Disintegrative Disorder (CDD): a case report
6天前
已完结
Analysis of homocysteine levels in carriers with MMACHC gene variants
26天前
已完结
[A case of 16p13.11 microdeletion syndrome with febrile convulsion as the main manifestation]
7个月前
已完结
The epidemiology of drug‐resistant epilepsy: A systematic review and meta‐analysis
7个月前
已完结
A novel microduplication in INPP5A segregates with schizophrenia spectrum disorder in the family of a patient with both childhood onset schizophrenia and autism spectrum disorder
7个月前
已完结
First pathogenic non-coding variant in MMACHC: a functional deletion in the 5′-UTR associated with cobalamin C deficiency
8个月前
已完结
Identification of Novel Protein Biomarkers for Myasthenia Gravis by Integrating Human Proteomics with Genetic Instruments
10个月前
已完结
Identification of a Splicing Variant c.3813-3A>G in NPHP3 by Reanalysis of Whole Exome Sequencing in a Chinese Boy with Nephronophthisis
11个月前
已完结
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