Lv3
280 积分 2024-02-27 加入
Concurrent Hearing and Genetic Screening of 180,469 Neonates with Follow-up in Beijing, China
1个月前
已完结
Molecular characteristics of α+-thalassemia (3.7 kb deletion) in Southeast Asia: Molecular subtypes, haplotypic heterogeneity, multiple founder effects and laboratory diagnostics
1年前
已完结
Molecular characterization and PCR detection of a deletional HPFH: Application to rapid prenatal diagnosis for compound heterozygotes of this defect with ?-thalassemia in a Chinese family
1年前
已完结
十个缺失型β-地中海贫血家系的产前诊断
1年前
已完结
十个缺失型β-地中海贫血家系的产前诊断
1年前
已关闭
Detection of α-globin gene deletion and duplication using quantitative multiplex PCR of short fluorescent fragments
1年前
已完结
Rapid analysis of -3.7 thalassaemia and anti 3.7 triplication by enzymatic amplification analysis
1年前
已完结
Validation of a reverse-hybridization StripAssay for the simultaneous analysis of common α-thalassemia point mutations and deletions
1年前
已完结
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