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Author:(Donglan ZHU)

1.Clinical Observation of Qi-blood-supplementing Needling for LeukopeniaAfter Chemotherapy for Breast Cancer

Donglan ZHU ; Haiyan Lü ; Yingyan Lü ; Leijuan WU

Shanghai Journal of Acupuncture and Moxibustion 2016;35(8):964-966

2.Application of laparoscopic simulators in the teaching of breast augmentation with endoscope assis-tant

Ji ZHU ; Jia LIU ; Donglan ZHUO ; Zhiqing ZHAO ; Chunyu XUE

Chinese Journal of Medical Education Research 2016;15(12):1243-1245,1246

3.The survey and intervention measures for the stress reaction in double- balloon enteroscopy

Haihua HUANG ; Jie PAN ; Liming ZHU ; Jie JIN ; Donglan WENG ; Biyun YE ; Guofeng MIAO

Chinese Journal of Practical Nursing 2010;26(7):20-22

4.Application of near infrared spectroscopy combined with particle swarm optimization based least square support vactor machine to rapid quantitative analysis of Corni Fructus.

Xuesong LIU ; Fenfang SUN ; Ye JIN ; Yongjiang WU ; Zhixin GU ; Li ZHU ; Donglan YAN

Acta Pharmaceutica Sinica 2015;50(12):1645-51

5.Diagnosis and differential diagnosis of nodular lymphocyte-predominant Hodgkin's lymphoma.

Yanhui LIU ; Xiongzeng ZHU ; Hengguo ZHUANG ; Hanliang LIN ; Qiuliang WU ; Guangyu JIANG ; Yingying GU ; Donglan LUO ; Xinlan LUO

Chinese Journal of Pathology 2002;31(3):227-230

6.Significance and case analysis of FMR1 mutation screening during early and middle pregnancy.

Qinying CAO ; Weihong MU ; Donglan SUN ; Junzhen ZHU ; Jun GE ; Yuanyuan PENG ; Jing ZHANG

Chinese Journal of Medical Genetics 2021;38(5):450-453

7.Genetic diagnosis of a case of Smith-Magenis syndrome due to a rare small-scale deletion.

Baodong TIAN ; Donglan YU ; Guangli WANG ; Bingyi HUANG ; Chunjiang ZHU

Chinese Journal of Medical Genetics 2022;39(9):1005-1010

8.Prenatal diagnosis and genetic counseling in two pedigrees affected with infantile polycystic kidney disease due to PKHD1 gene mutations.

Qinying CAO ; Weixia ZHANG ; Jun GE ; Donglan SUN ; Qingqi FENG ; Caixia LI ; Yucui MENG ; Junzhen ZHU

Chinese Journal of Medical Genetics 2019;36(8):765-768

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