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.
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
3.
PRENATAL DIAGNOSIS OF β-THALASSEMIA--Ⅱ.PRENATAL GENE DIAGNOSIS BY HAPLOTYPING OF THE β-GLOBIN GENE CLUSTER
β-地中海贫血的产前诊断——Ⅰ.用β-珠蛋白基因簇单体型分析进行产前基因诊断
4.
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
5.
Investigation the carrier rate and fetal diagnosis of thalassemia in zhanjiang city
湛江地区地中海贫血基因携带率及产前基因诊断的研究
6.
MOLECULAR BASES OF β-THALASSEMIA AND PRENATAL DIAGNOSIS 11 FETUSES AT RISK FOR β-THALASSENIA IN EAST AREA OF SICHUAN
四川东部地区β地中海贫血分子基础及产前基因诊断11例
7.
Clinical application of prenatal gene diagnosis of Duchenne and Becker muscular dystrophy
假肥大型肌营养不良症产前基因诊断的临床应用
8.
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
9.
Prenatal Gene Diagnosis for the Duchenne Muscular Dystrophy Risk Fetus by Molecule Markers
应用分子标记对Duchenne型肌营养不良胎儿的产前基因诊断
10.
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
11.
The Research of Prenatal Gene Diagnosis of DMD Using Fetal Erythro Blasts from Maternal Peripheral Blood;
孕妇外周血中胎儿有核红细胞在DMD胎儿产前基因诊断中的应用研究
12.
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
13.
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
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.
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
16.
Rapid Prenatal Detection of Down Syndrome by Homologous Gene Quantitative PCR;
同源基因定量PCR方法产前快速诊断Down综合征
17.
The Methodology on Prenatal Screening and Gene Diagnosis for Down s Syndrome;
唐氏综合征产前筛查及基因诊断的方法学研究
18.
Gene mutation analysis in a patient with Wiskott-Aldrich syndrome and prenatal diagnosis for a fetus in the family
一例Wiskott-Aldrich综合征致病基因突变分析及产前诊断