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Keyword [Heterozygous]
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1. Study Of Activation Of BTAK Expression In Primary Ovarian Surface Epithelial Cells Carrying Heterozygous BRCA Mutation And Tumorigenesis Of Ovarian Carcinoma
2. Interleukin-2 And Platelet Activation In The Pathogenesis Of Ulcerative Colitis
3. Heterozygous Biotechnology Of Antibiotics Neomycin And 68 Active Metabolites Of Fungal Chemical Research
4. Detection Of The Expression Of Gene TSG101 And Its Splice Variants In Peripheral Blood Cells Of Healthy People
5. A Report For Partial Lipoatrophy Due To A Heterozygous LMNA R482Q Mutation
6. The Investigation Of Experimental Optimizion Of G6PD/6PGD Direct Ratio Enzymic Activity Method
7. Research On The Application Of Quantitative Pyrosequencing Of Heterozygous Single Nucleotide Polymorphism For Rapid Prenatal Diagnosis Of Down Syndrome
8. Research On The Application Of Quantitative Pyrosequencing For Rapid Diagnosis Of DOWN'S Syndrome
9. Establishment And Preliminary Study Of Animal Model Of Asymptomatic Hyperuricemia
10. Research On The Application Of Quantitative Pyrosequencing For Rapid Diagnosis Of Down's Syndrome
11. Adenovirus - A Virus Heterozygous Carrier Construction And Virus Preparation
12. Signaling Role Of Prokineticin2/Prokineticin Receptor2in Female Reproduction System
13. Mutation Analysis In330Chinese Cases With DMD/BMD And Genetic Analysis In A Fetus With Compound Heterozygous DMD Mutations
14. Analysis Of TGFBI Gene Mutation In A Chinese Family With Lattice Corneal Dystrophy I
15. Exome Sequencing Identifies Novel Compound Heterozygous Mutations In SPG11That Cause Autosomal Recessive Hereditary Spastic Paraplegia
16. Sequence Analysis Of The Upstream Regulation Sequences Of GJB2Based On GJB2235delC Heterozygous Deaf Patients
17. Sequence Analysis Of The Upstream Regulation Sequences Of GJB2Based On GJB2235DelC Heterozygous Deaf Patients
18. A New Compound Heterozygous Mutation In CYP17A1 Gene Causes 17α-hydroxylase Deficiency And Pedigree Study
19. The Correlation Research Between WD Carriers’ Genotyping And Laboratory Index
20. Molecular Genetics Of A Chinese Family With Avellino Corneal Dystrophy
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