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1. Study Of Morphologic, Immuophenotypic And Genetic Features And Their Diagnostic Significance For Sporadic Adult Papillary Thyroid Carcinoma
2. Study Of FUS-CHOP Fusion Gene And Its Diagnostic Significance For Myxoid/round Cell Liposarcomas
3. Validation On The Interaction Between Jumping Translocation Breakpoint Protein And Envelope Protein Of Hepatitis B Virus
4. Establishment And Characterization Of A Human Acute Myelocytic Leukemic Cell Line, SH-2, Carrying Non-balanced T(16;17) (q24;q12) Chromosomal Translocation
5. The Study On Dietary Reference Intakes Of Protein For Chinese Female Youths
6. 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
7. Breakpoint Mapping And Its Significance On Large Deletions Of Chromosome9p21
8. Quantitative Analysis Of Glaucoma Lesions Based On OCT Images
9. Cloning And Application Of Dystrophin Gene Deletion Junctions
10. Rat Cocaine Self-administration Model Of The Establishment And Administration Of The Program On The Desirability,
11. Studies On Extended-spectrum β-lactamases And Outer Membrane Protein In Enterobacteriaceae
12. Characterization Of Copy Number Variations At The Single-base-pair Level Through WGS And The Mutational Mechanisms Revealed
13. Development Of Enrofloxacin Susceptibility Breakpoint For Salmonella In Pigs
14. Study On Y Chromosome Microdeletions And Pedigree Analysis In Patients With Idiopathic Azospermia And Oligozoospermia
15. The PK/PD Study Of Sequential Therapy Of Cefetamet And Cefetamet Pivoxil Hydrochloride
16. Analysis Of Effect Of Ovulation Induction Cycle Of Balanced Chromosomal Translocation Carriers
17. Delineation of molecular bases of chromosomal and Mendelian phenotypes
18. Research On The Impact Of Catastrophic Health Expenditure On Expected Income Level Of Rural Residents In Western China
19. Research On The Impact Mechanism Of Retirement On Health
20. Methodology Study On Detection Of Structural Variation Breakpoint From Next-generation Sequencing Data
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