1.
Genetic Diagnosis of Down Syndrome and Preliminary Study on Non-Invasive Prenatal Diagnosis of Down Syndrome;
唐氏综合征的基因诊断及其无创性产前基因诊断的初步研究
2.
The Improvement and Application in the Techniques of the Non-invasive Prenatal Genetic Diagnosis;
无创性产前基因诊断技术的改进与应用
3.
Use of Fetal Specific Antbody-HbF(γ Chain) to Detect Fetal Erythroblasts for Non-invasive Prenatal Diagnosis of DMD;
应用胎儿特异性抗体HbF（γ链）标记法无创性产前基因诊断DMD
4.
Investigation of Non-Invasive Prenatal Genetic Diagnosis for B Thalassaemia Using Single Fetal Nucleated Erythrocytes from Maternal Blood;
孕妇外周血中单个胎儿有核红细胞在β地中海贫血无创性产前基因诊断中的应用研究
5.
Research of Noninvasive Prenatal Diagnosis of Thalassemia Using Size-Fractionated Cell-Free Fetal DNA in Maternal Plasma;
利用孕妇外周血浆中小片段游离胎儿DNA进行无创性地中海贫血产前基因诊断的研究
6.
Feasibility study of Hypermethylated ERG as a marker of noninvasive prenatal diagnosis of Down's syndrome
ERG甲基化作为无创产前诊断唐氏综合征标记的可行性研究
7.
The Study of the Biochips for Non-invasive Prenatal Diagnosis on Inherited Disorder;
无创性产前诊断遗传性疾病的生物芯片的研究
8.
Molecular Diagnosis and Prenatal Diagnosis of Three Monogenic Diseases
三种单基因病的分子诊断与产前诊断
9.
Gene Sequencing and Prenatal Diagnosis of Spinal Muscular Atrophy;
脊髓性肌萎缩症基因测序及产前基因诊断
10.
Genetic Counseling and Prenatal Diagnosis for Hearing Loss Based on Genetic Testing;
基于基因诊断的耳聋遗传咨询与产前诊断
11.
The Study of Enrichment and Isolation of Fetal Cells From Peripheral Maternal Blood and Its Application in Noninvasive Prenatal Diagnosis;
从孕妇外周血分选胎儿细胞行无创性产前诊断的研究
12.
The Study of Detection on β-thalassemia by Chip-based Capillary Electrophoresis and Noninvasive Prenatal Diagnosis;
芯片毛细管电泳检测β-地中海贫血及无创性产前诊断的研究
13.
Noninvasive prenatal diagnosis of fetal ABO blood genotype using fetal DNA in maternal plasma
孕妇血浆中游离DNA在无创性产前诊断胎儿ABO血型中的应用
14.
A Study on the Gene Test and Prenatal Diagnosis for Thalassemias
地中海贫血基因诊断和产前诊断的研究
15.
Noninvasive Prenatal Diagnosis of Congenital Toxoplasma Infection Using Fetal Nucleated Erythrocytes Circulating in Maternal Peripheral Blood;
利用孕妇外周血中胎儿有核红细胞无创性产前诊断先天性弓形虫感染的研究
16.
Significance of Gene Diagnosis and Prenatal Diagnosis for Oculocutaneous Albimism TypeⅠ(OCA1)
眼皮肤白化病Ⅰ型的基因诊断及产前诊断的意义
17.
Noninvasive Prenatal Diagnosis of Chromosome Aneuploidies Using Fetal Nucleated Erythrocytes Circulating in Maternal Peripheral Blood;
利用孕妇外周血中胎儿有核红细胞无创性产前诊断染色体非整倍体异常
18.
Establishment of New Detection Techniques for Fetal Paternal Point Mutations in Maternal Plasma and Their Significance in Noninvasive Prenatal Diagnosis;
母体血浆中胎儿DNA点突变新型检测技术在无创性产前诊断中价值的研究