1.
Study on Screening, Diagnosis and Intellectual Development Status in Children with Chromosome 22q11 Deletion Syndrome
染色体22q11微缺失综合征的筛查与诊断及其智能发育状况的研究
2.
Diagnosis of 22q11 deletion and duplication in congenital heart disease by multiplex ligation-dependent probe amplification
多重连接探针扩增技术在先天性心脏病22q11微缺失/微重复综合征诊断中的应用
3.
Study on the Relationship between 22q11 Microdeletion and Simple Congenital Heart Disease;
单纯性先天性心脏病22q11微缺失的研究
4.
Rapid Detection of the 22q11 Deletion with Quantitative Real-time PCR;
实时荧光定量PCR快速诊断22q11微缺失
5.
Detection of Y chromosome microdeletions in azoospermic patients with Klinefelter′s syndrome
Klinefelter综合征Y染色体微缺失的检测
6.
Analysis of the clinical phenotype and pathogenesis in seven children with 22q11.2 deletion syndrome.
22q11.2微缺失综合征7例相关临床表型及病因分析
7.
Establishment and Application of Genetic Diagnostic System for Eight Chromosome Microdeletion Syndromes by Fluorescence in Situ Hybridization;
8种微缺失综合征荧光原位杂交诊断体系的建立与应用
8.
Progresses on the genetic study of 22q11 deletion syndrome
22号染色体长臂近端微片段缺失综合征的遗传学研究
9.
acquired immunity deficiency syndrome
获得性免疫缺乏综合征
10.
sideropenic dysphagia syndrome
缺铁性吞咽困难综合征
11.
secondary antibody deficiency syndrome
继发性抗体缺乏综合征
12.
acquired immunodeficiency syndrome, AIDS
获得性免疫缺陷综合征
13.
Kallman syndrome
性幼稚－失嗅综合征
14.
Deletion of p15 Gene and Promoter Methylation in Myelodysplastic Syndromes
骨髓增生异常综合征p15基因的表达缺失和启动子甲基化
15.
Deletion of the p15 Gene and Promoter Methylation in the Bone Marrow of patients with Myelodysplastic Syndromes
骨髓增生异常综合征患者骨髓p15基因的表达缺失与启动子甲基化
16.
Establishment of RT-PCR for detection of nsp2 deletion porcine reproductive and respiratory syndrome virus
猪繁殖与呼吸综合征病毒nsp2基因缺失株RT-PCR检测方法的建立
17.
Muscle segment homeobox gene-1 and non-syndromic hypodontia
同源异型盒基因-1与非综合征型多数牙先天性缺失
18.
On College Student s Network Honest Lost and It s Comprehensive Treatment;
浅谈大学生网络诚信缺失及综合治理