The diagnosis factor of the sustainable development level in the Heihe oasis is determined by the factor analysis method in this paper.
本文通过因子分析方法确定出黑河绿洲可持续发展水平的诊断因子,并对其进行实力评估。
Gene diagnosis and clinical features of facioscapulohumeral muscular dystrophy;
50例面肩肱型肌营养不良症的基因诊断与临床特征
Rapid gene diagnosis for commom systemic Candida infection;
常见深部念珠菌感染快速基因诊断
Application of the BglⅡ-BlnⅠdosage test to gene diagnosis of facioscapulohumeral muscular dystrophy 1A gene;
BglⅡ-BlnⅠ剂量检测方法在面肩肱型肌营养不良症1A基因诊断中的应用
Clinicopathological analysis and genetic diagnosis of subcutaneous panniculitic T-cell lymphoma;
皮下脂膜炎样T细胞淋巴瘤的病理分析及基因诊断
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
Herein,we briefly describe the latest advances of the research on the genetic diagnosis of monogenetic inherited .
本文将概述单基因遗传性内分泌代谢病的基因诊断及其临床应用方面的最新研究进展。
By this novel approach, not only DNA sequencing and gene expression analysis but also gene diagnoses, study of gene singlenucleotide polymorphisms(SNPs) and new medicine screening can be performed.
DNA芯片技术目前已用于基因重复测序、基因表达分析、新基因的发现、基因单核苷酸多态性 ( SNPs)研究、基因诊断、药物筛选等领域 ,而且其应用范围还在不断扩展。
Significance for TORCH infection in etiological diagnosis of neonatal hyperbilirubinemia;
TORCH感染在新生儿高胆红素血症病因诊断中的意义
Etiological Diagnosis of 34 Patients with Suspected Obscure Small Intestinal Bleeding -- A Comparative Study of Double-balloon Push Enteroscopy and Enteroclysis;
34例不明原因疑小肠出血的病因诊断——推进式双气囊小肠镜与小肠钡灌检查对比研究
Application of Breast High-frequency Ultrasonography in Etiological Diagnosis of Girls with Precocious Puberty;
乳腺高频超声检查在女童性早熟病因诊断中的应用
Diagnosis of small leaf symptom of peach in Northwestern Fujian province and factors inducing the regional outbreak of this symptom;
闽西北桃小叶症病因诊断与区域性骤发诱因
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
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
Diagnosis of ADPKD by Using Gene Chips;
应用基因芯片技术对ADPKD进行基因诊断
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
A method of quickly sequencing DNA in gene diagnosis
基因诊断中DNA序列的快速检测法
Study of Gene Diagnosis of Vitamin D Resistant Rickets;
抗维生素D佝偻病PHEX基因诊断研究
The Application of Microchip Electrophoresis for Gene Diagnosis;
微流控芯片在基因诊断中的应用研究
A Study of Genetic Diagnosis on HSV-1, HSV-2, EBV and HCMV;
HSV-1，HSV-2，EBV和HCMV的基因诊断研究
A study on the gene diagnosis of thalassemias in 59 cases
59例地中海贫血患者的基因诊断研究
Clinical and Gene Diagnosis on Menkes Disease in Two Families
Menkes病2家系临床和基因诊断研究
The Study of Gene Diagnosis of Monogenic Diseases and It's Application;
单基因遗传病的基因诊断及其应用研究
Study on the Gene Diagnosis and the Genotype-Phenotype Correlation of Wilson Disease;
Wilson病基因诊断及基因型与表型关系的研究
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
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
Human Genome Project,Post-genome Research and Gene Medicine --New Century of Diagnosis,Pharmaceutics and Therapy with Gene Technique;
人类基因组计划、后基因组研究与基因医学——基因诊断、基因制药与基因治疗的新世纪
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
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
The Value of Detection of Survivin mRNA in Malignant Pleural Effusion;
survivin基因在恶性胸腔积液诊断中的价值