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1. Fine Mapping And Candidate Genes Study Of PSORS1 In Chinese Population
2. Reliable Detection Of Paternal SNPs Within Deletion Breakpoints For Non-invasive Prenatal Exclusion Of Homozygosity For α~0-thalassemia Using Cell-free Fetal DNA In Maternal Plasma
3. Study Of Sensitive Breakpoints Within The D-loop Region Of MtDNA
4. The Detection Of Novel Fusion Genes Related With The AML1 Gene And The Breakpoints
5. Application Of Next-generation Sequencing On Study Genomic Structural Variants
6. Development and Application of Next-Generation Sequencing Methods to Profile Cellular Translational Dynamic
7. Identification and Characterization of Novel Micro-Alterations and Overt Cytogenetic Breakpoints Using High Resolution Mate-Pair Sequencing in Primary Myelofibrosis
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