1.
Rapid Prenatal Detection of Down s and 18 Trisomy Syndromes by Quantitative Fluorescent Polymerase Chain Reaction with Short Tandem Repeat Markers;
荧光定量PCR快速诊断21-三体综合征及18-三体综合征
2.
Rapid Diagnosis of Trisomy 13 and Trisomy 18 by Quantitative Fluorescent PCR(QF-PCR)
荧光多重PCR技术在13-三体综合征及18-三体综合征诊断中的应用
3.
The practical value with antenatal filtering examination to diagnosis trisomy syndrome
产前筛查在诊断18-三体综合征中的应用价值
4.
Electrophysiologic Studies (EPS) and Treatment in 18 Patients with Preexcitation Syndrome (PS)
18例预激综合征的电生理检查及治疗
5.
Clicnial analysis of 18 patients with recurrent Guillain-Barre syndrome
复发性吉兰-巴雷综合征18例临床分析
6.
Clinical analysis on 18 cases of acute respiratory distress syndrome
急性呼吸窘迫综合征18例临床分析
7.
Clinical analysis of 18 cases of Parkinson disease or Parkinson syndrome with restless legs syndrome
帕金森病或帕金森综合征合并不宁腿综合征18例临床分析
8.
Clinical Significance of Interleukin-18/Interleukin-10 Ratioin Patients with Acute Coronary Syndrome;
急性冠脉综合征患者IL-18/IL-10比值的临床意义
9.
Rapid Diagnosis of 21 Trisomy Syndrome by SYBR Green I Homologous Genes Quantitative Polymerase Chain Reaction (HGQ-PCR);
SYBR Green I 同源基因定量PCR快速诊断21-三体综合征
10.
Ultrasound screening for trisomy 21 syndrome at 11-13~(+6) gestational weeks
超声在孕11-13~(+6)周筛查21-三体综合征中的作用
11.
Ultrasonographic Screening for Trisomy 21 After 11 to 13~(+6) weeks of Gestation
孕11～13~(+6)周超声筛查胎儿21-三体综合征的研究
12.
Hematological Characteristics and Prognosis of Myelodysplastic Syndrome with Sole Trisomy 11
单纯11三体骨髓增生异常综合征的血液学特征与预后
13.
Meta-analysis of prenatal screening for trisomy 21 using nuchal translucency measurement with serum markers
血清学指标结合颈部透明膜产前筛查21-三体综合征的Meta分析
14.
secondary antibody deficiency syndrome
继发性抗体缺乏综合征
15.
ectopic pinealoma syndrome
异位松果体瘤综合征
16.
Diagnosis and treatment of 56 cases of Mirizzi's syndrome
Mirizzi综合征56例诊治体会
17.
Experiences on Mirizzi syndrome in 21 cases
Mirizzi综合征21例诊治体会
18.
Diagnosis and treatment of Mirizzi's syndrome
Mirizzi综合征28例诊治体会