高选山东大学主页平台管理系统--中文主页

更多

` 中文
- English

高选

职称：副主任技师
所在单位：生殖医学研究中心

教师拼音名称：gaoxuan
入职时间：1989-07-01
所在单位：生殖医学研究中心
性别：女
在职信息：在职
是否在职：1

论文成果

[16] 傅海龙. Y染色体嵌合体核型患者男性生育功能参数特征分析.. 社区医学杂志, 19, 547, 2021.
[17] 陈虹. 染色体制备中冷藏悬液和新鲜悬液滴片的差异性研究.. 医学检验与临床, 2021.
[18] 杨斯桀. PDCA循环在男科实验室中缩短精液样本周转时间的应用. 《中华男科学杂志》, 27, 31, 2022.
[19] 赵冰清. 基于辅助生殖人群的复发性流产夫妇染色体核型回顾性分析. 山东大学学报（医学版）, 2021.
[20] 刘雯. Analysis of STAG3 variants in Chinese non-obstructive azoospermia patients with germ cell maturation arrest. Scientific Reports, 11, 2021.
[21] 黄色新. Complex preimplantation genetic tests for Robertsonian translocation, HLA, and X-linked hyper IgM syndrome caused by a novel mutation of CD40LG gene. Journal of assisted reproduction and genetics, 37, 2025, 2020.
[22] 李婷. 部分型圆头精子症患者精液常规参数及精子形态分析. 《中华男科学杂志》, 23, 57, 2017.
[23] 徐佩文. A Novel Splicing Mutation in the FBN2 Gene in a Family With Congenital Contractural Arachnodactyly. FRONTIERS IN GENETICS, 11, 2020.
[24] 牛玉萍. A nonsense variant inFBN1caused autosomal dominant Marfan syndrome in a Chinese family: a case report. BMC MEDICAL GENETICS, 21, 2020.
[25] 黄色新. Complex preimplantation genetic tests for Robertsonian translocation, HLA and X-Linked Hyper IgM Syndrome caused by a novel mutation of CD40LG gene. JOURNAL OF ASSISTED REPRODUCTION AND GENETICS, 2020.
[26] 邹洋. 微滴式数字PCR在脊肌萎缩症基因检测和产前诊断中的应用. 中华医学遗传学, 2017.
[27] 徐佩文. A Novel Splicing Mutation in the FBN2 Gene in a Family With Congenital Contractural Arachnodactyly. FRONTIERS IN GENETICS, 2020.
[28] 黄色新. 一例SMN1基因型疑为“2+0”型脊肌萎缩症家系的确认. 中国优生与遗传杂志, 2016.
[29] 徐佩文. A novel splicing mutation in the PKD1 gene causes autosomal dominant polycystic kidney disease in a Chinese family. BMC Medical Genetics, 19, 2018.
[30] Xu, Peiwen. A novel splicing mutation in the PKD1 gene causes autosomal dominant polycystic kidney disease in a Chinese family: a case report. BMC MEDICAL GENETICS, 19, 2018.

共94条 2/7

首页上页下页尾页页

扫一扫用手机查看