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Keyword [chromosome microarray]
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1. Application Of Chromosome Microarray Investigated Fetuses With Common Urinary Abnormalities
2. Application Of Chromosome Microarray Analysis (CMA) Investigated33Patients With Congenital Cleft Lip And Palate
3. The Cause Of The Development Of Embryonic Development Is Based Onthe Combination Of Immuno-antibody And Partial Environmental Factoes
4. A Series Of Studies On Prenatal Investigation And Diagnosis Of Genetic Etiology With Congenital Cleft Lip And Palate
5. Effect Of Compound Heterozygous ASXL3 Gene Mutation In A Mouse Model By Integrated Bioinformatic Analysis And Its Interaction With SOCS3 And PSD95
6. Analysis Of Existing Screening Techniques And Screening Of New Marker Genes For Down Syndrome
7. Efficiency Of Whole Genome Sequencing Applied For Detecting Chromosomal Anomalies In Non-Invasive Prenatal/Preimplantation Diagnosis
8. The Investigation Of Genetic Etiology Of Unexplained Intellectual Disability/Global Developmental Delay
9. Analysis Of The Correlation Between Fetal Chromosomal Abnormalities And Missed Abortion
10. Chromosomal Microarray Analysis Of Advanced Age Pregnancy And Fetal Congenital Heart Diseases
11. Analysis Of Chromosomal Aberrations In Fetuses With Heart Defects
12. Analysis Of Chromosomal Aberrations In Fetuses With Growth Restriction
13. Ultrasonic Diagnosis Of Fetal Aortic Arch Anomalies And Its Clinical Study On 22q11 Microdeletion
14. Analysis Of Fetal Chromosome Detection Results In 3226 Pregnant Women With Different Prenatal Diagnosis Indications
15. Application Of Chromosome Microarray Analysis In Prenatal Diagnosis Of Fetus With Abnormal Ultrasound Softmarkers
16. Analysis Of Etiology Of Premature Ovarian Insufficiency In Children And Adolescent
17. Application Of Chromosomal Microarray Analysis In Fetuses With Neurodevelopmental Abnormalities
18. Analysis Of Chromosome Microarray Results In Adverse Reproductive History And Fetuses With Ultrasound Abnormalities
19. Analysis Of Related Risk Factors Of Missed Abortion
20. Noninvasive Prenatal Testing For Fetal Chromosomal Copy Number Variation
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