forensics
1. if: 5.637 products:microreader™ 23sp id system
analysis of genetic polymorphisms and mutations at 23 autosomal str loci in guangdong han population. forensic science international: genetics, 2019.
2. if: 5.637 products:microreader™ 23sp id system
validation of the microreader™ 23sp id system: a new str 23-plex system for forensic application. forensic science international: genetics, 2017.
3. if:5.637 products:microreader™ 23sp id system
multistep microsatellite mutation at d18s51 locus in a parentage testing case. forensic science international: genetics supplement series, 2017.
4. if: 5.637 products:microreader™ 23sp id system
genetic polymorphism of 22 autosomal str markers in a han population of southern china. forensic science international: genetics, 2016.
5. if: 5.637 products:microreader™ 23sp id system
genetic polymorphisms of 22 autosomal str loci in chinese han population. forensic science international: genetics supplement series, 2015.
6. if: 2.094 products:microreader™ 19x id system
genetic characterization of 19 x-strs in sierra leone population from freetown. int j legal med, 2020.
7. if: 1.276 products:microreader™ 19x id system
loss of heterozygosity detected at three short tandem repeat locus commonly used for human dna identification in a case of paternity testing. legal medicine, 2017.
clinical research
1. if:19.783
2. if:8.783
3. if: 4.526 products:msi detection kit
a novel and reliable method to detect microsatellite instability in colorectal cancer by next-generation sequencing. the journal of molecular diagnostics, 2017.
4. if:3.892 products:fxs detection kit
a novel deletion to normal size in the sperm of a fragile x full mutation male. clin genet.
5. if: 3.517 products:msi detection kit
effect of tumor location on clinicopathological and molecular markers in colorectal cancer in eastern china patients: an analysis of 2,356 cases. front genet, 2020.
6. if: 2.535 products:msi detection kit
mismatch repair status between primary colorectal tumor and metastatic tumor, a retrospective consistent study. bioscience rep, 2019.
7. if:1.813
fragile x syndrome screening in chinese children with unknown intellectual developmental disorder. bmc pediatrics.
8. if: 1.26 products:
molecular and cytogenetic analysis of infertile hakka men with azoospermia and severe oligozoospermia in southern china.journal of international medical research, 2019.
9. if:0.799
loss of heterozygosity at the human leukocyte antigen locus in thymic epithelial tumors.thoracic cancer.