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Keyword [Chromosome]
Result: 181 - 200 | Page: 10 of 10
181. Study On The Relationship Between Microsatellite Abnormity At Chromosome 17 And Lung Cncer
182. Relationship Between Human Hepatocellular Carcinoma And Deletion At The P53 Gene Locus As Well As The Expression Of Occludin
183. Loss Of Heterozygosity And Microsatellite Instability On Chromosome 3p14 In Cervical Carcinoma
184. The Study Of Sister Chromatid Exchange Assay And Micronucleus Assay As Biomarkers For Evaluating Radiotherapy Induced Cytogenetic Damage Of Cervical Carcinoma Patients
185. Two New Scant Hair Mice Induced By ENU And Mapping Of The Mutant Gene On Chromosome
186. The Observation And The Analysis Of Chromosome Aberrations In Previous Victims Of Radiation Accident By AFM
187. Cytogenetic Analysis Of 45 Patients With Myelodysplastic Syndrome
188. Study On The Pharmacognosy Of Two Species Plants Of Physalis Of China
189. Genetic Polymorphisms Of Y-STR DYS19,DYS390 In Han Nationality Of NanChang
190. The Application Of Fluorescence In Situ Hybridization Technology (FISH) To The Diagnosis Of Chromosome Abnormality In Genetic Diseases And Prenatal Diagnosis
191. Alteration Of Genes In Chromosome 3q Of Esophageal Carcinoma Analyzed By BAC Probes
192. Cytogenetic Analysis Of Urinary Bladder Cancer Combining Comparative Genomic Hybridization And Chromosome-specific Painting
193. Effects Of Selenium On Genetic Damage Induced By Mitomycin-C In Human Peripheral Lymphocytes
194. Improvement And Application Of Spectral Karyotyping In Detection Of The Complex Chromosome Abnormalities In Prenatal Diagnosis
195. Preimplantation Genetic Diagnosis For Patients With Chromosome Structure Abnormalities
196. Relationship Between Genetic Instability Of Chromosome 17q21 And Clinical Pathological Behaviors In Chinese With Gastric Cancer
197. Establishment Of Repetitive Multicolour Fluorescence In Situ Hybridization And Study In Esophageal Squamous Cell Carcinomas
198. Systematic Analysis Of Huangqi Seeds And Its Adulterants
199. Construction Of Bacterial Artificial Chromosome Vectors Containing Human Tissue-type Plasminogen Activator Mutant Gene Specially Expressed In Mammary Gland With Red Recombination System
200. Investigation Of Y-chromosome Microdeletions In Male Infertility
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