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- Loss of heterozygosity detected at three short tandem repeat locus commonly used for human DNA identification in a case of paternity testing
- Genetic and chromosomal variation-caused inconsistencies in two parental tests
- Developmental validation study of a 24-plex Y-STR direct amplification system for forensic application
- Genetic characterization of 19 X-STRs in Sierra Leone population from Freetown
- Development one novel multiplex PCR system for forensic individual identification using insertion/deletion polymorphisms
Thalassaemia intermedia caused by coinheritance of a β‐thalassaemia mutation and a de novo duplication of α‐globin genes in the paternal allele
发布时间：
2020-04-30 02:41
来源：北京阅微基因技术有限公司
| 领域： | 法医,刑侦 | ||
| 资料类型： | 其他资料 | ||
| 资料文件名 | 下载 |
|---|---|
Thalassaemia intermedia caused by coinheritance of a β‐thalassaemia mutation and a de novo duplication of α‐globin genes in the paternal allele |
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IF: 5.206 相关产品：Microreader™ 20A ID System
Thalassaemia intermedia caused by coinheritance of a β‐thalassaemia mutation and a de novo duplication of α‐globin genes in the paternal allele. BRIT J HAEMATOL, 2019.
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