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Keyword [Prenatal Diagnosis]
Result: 21 - 40 | Page: 2 of 10
21.
Development Of Techniques For Prenatal Genetic Diagnosis Of Common Aneuploidy And Monogenic Diseases
22.
Study On A Method Using Fetal Nucleated Erythrocytes Screened From Maternal Peripheral Blood By Biological Nanotechnology For Diagnosis Of Down Syndrome
23.
Study On Prevention And Intervention For Hereditary Hearing Loss Based On Genetic Testing
24.
Noninvasive Prenatal Diagnosis Of Down Syndrome And Function Analysis Of Down Syndrome Related Genes
25.
The Evaluation Of Serial Invasive Prenatal Diagnostic Techniques
26.
Congenital Heart Disease Prevention
27.
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
28.
Study On Clinical Performance Of Method BACs-on-Beads
29.
Synpolydactyly (SPD) In A Chinese Kindred:Clinical Features,Mutation Detection, Prenatal Ultrasonographic And Molecular Diagnosis
30.
Rapid Gene Diagnosis Of Down Syndrome By Quantitative Polymerase Chain Reaction
31.
Rapid Detection Of Down Syndrome By Polymerase Chain Reaction-Simple Sequence Length Polymorphism (PCR-SSLP)
32.
Experimental Study On The Transmission Approach And Detecting Fetal Genetic Infonmation In Maternal Blood
33.
Dynamic Variation Of (CAG)n Repeats In SCA
1
And SCA
3
/MJD Genes Studying And Applicating In The Clinical Diagnosis
34.
Detection Fetal DNA From Maternal Peripheral Blood And The Application Of Fetal DNA In Noninvasive Prenatal Diagnosis For Down's Syndrome
35.
The Study Of Detecting β-thalassaemia Mutations From A Single Cell
36.
Use Of Fetal Specific Antbody-HbF(γ Chain) To Detect Fetal Erythroblasts For Non-invasive Prenatal Diagnosis Of DMD
37.
Detection Fetal DNA From Maternal Peripheral Blood And The Application Of Fetal DNA In Noninvasive Prenatal Diagnosis
38.
To Establishe And Evaluate Methods Based On Capillary Electrophoresis And Denaturing High-performance Liquid Chromatography Used In Thalassemia Diagnosis
39.
The Application Of Fluorescence In Situ Hybridization Technology (FISH) To The Diagnosis Of Chromosome Abnormality In Genetic Diseases And Prenatal Diagnosis
40.
Expression Of Adrenoleukodystrophy Protein In E.coli And Molecular Diagnosis Of Adrenoleukodystrophy
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