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Keyword [Noninvasive prenatal]
Result: 21 - 40 | Page: 2 of 4
21. Construction Of The Method Based On Quantitative Detection Of Sex Chromosome For Non-invasive Screening Of Sex-linked Genetic Diseases
22. Use Of Free Fetal DNA In Maternal Plasma To Noninvasive Prenatal Diagnosis β-thalassemia Methods Research
23. Noninvasive Prenatal Screen Of Trisomy-21 Using Maternal Plasma Fetal Free MRNA Allelic Ratio
24. Noninvasive Prenatal Diagnosis Of Fetal RhD Status And Fetal FGFR3 Mutation Using MALDI-TOF MS
25. Combining The Effects Of Cell-free Circulating Tumor DNA With The Noninvasive Prenatal Testing Results Of Breast Tumor Patients By A Simulating Investigation
26. Screening And Identification Of Differentially Methylated Markers Between Maternal And Fetal DNA
27. Analysis Of PAH Gene Mutation Spectrum In Patients With Phenylketonuria In Northwest China And Preliminary Study Of Noninvasive Prenatal Diagnosis
28. Clinical Performance Of High-throughput Sequencing Technology In Prenatal Diagnosis
29. Investigation On Clinical Application Of Nextgeneration Sequencing Technology In China
30. The Application Value Of Noninvasive Prenatal Testing In Xinjiang Region
31. Noninvasive Prenatal Testing In The Clinical Application Evaluation Of Down's Syndrome
32. Detection Of Cell-free Fetal DNA In Maternal Plasma For Noninvasive Prenatal Screening Of Fetal Common Chromosomal Aneuploidy In Women Of Advanced Maternal Age
33. To Investig The Value Of Noninvasive Prenatal Testing In The Prenatal Diagnosis Of Fetal Chromosomal Aneuploidy
34. A Pilot Study Of Noninvasive Prenatal Paternity Tesing Based On STR And SNP Typing
35. The Application Value Of Noninvasive Prenatal Testing In The Detection Of Fetal Chromosomal Abnormalities In Ningxia
36. Genetic Analysis And Prenatal Diagnosis Of Congenital Adrenal Hyperplasia Due To 21-hydroxylase Deficiency
37. Noninvasive Prenatal Diagnosis For ?- Thalassemia Based On Next-generation Sequencing And Pseudo-tetraploid Genotyping
38. Genetic Susceptibility Gene And Noninvasive Prenatal Diagnosis Study Of Psychiatric Disorders And Inherited Neurological Diseases
39. Identification Of Molecular Etiology In Pedigrees With Inherited Hearing Loss And Study Of Noninvasive Prenatal Testing Of Hearing Loss
40. Analysis Of Genotype-Phenotype Correlations In Deafness Syndrome And Exploration Of Early Non-invasive Prenatal Testing Based On Endocervical Fetal Trophoblast
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