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28 积分 2025-07-02 加入
Characteristic features of the genotype and phenotype of hereditary spherocytosis in the Japanese population
5天前
已关闭
Exome sequencing confirms molecular diagnoses in 38 Chinese families with hereditary spherocytosis
2个月前
已完结
A tetranucleotide deletion in the ANK1 gene causes hereditary spherocytosis; a case of misdiagnosis
2个月前
已完结
The molecular basis of hereditary red cell membrane disorders
3个月前
已完结
Whole‐exome sequencing uncovered genetic diagnosis of severe inherited haemolytic anaemia: Correlation with clinical phenotypes
4个月前
已完结
Metabolomics profile and machine learning prediction of treatment responses in immune thrombocytopenia: A prospective cohort study
7个月前
已完结
Study on diagnostic‐sensitive markers of primary immune thrombocytopaenia in children based on plasma proteomics
7个月前
已完结
Targeted proteomics profiling reveals valuable biomarkers in the diagnosis of primary immune thrombocytopaenia
7个月前
已完结
The Correlation Between Clinical Phenotype and Genotype of Hereditary Spherocytosis
8个月前
已完结
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