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Date of Employment:1989-07-01

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[21] 黄色新. Complex preimplantation genetic tests for Robertsonian translocation, HLA, and X-linked hyper IgM.... 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 Arachnodactyl.... FRONTIERS IN GENETICS, 11, 2020.
[24] 牛玉萍. A nonsense variant inFBN1caused autosomal dominant Marfan syndrome in a Chinese family: a case re.... BMC MEDICAL GENETICS, 21, 2020.
[25] 黄色新. Complex preimplantation genetic tests for Robertsonian translocation, HLA and X-Linked Hyper IgM .... 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 Arachnodactyl.... 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.... BMC Medical Genetics, 19, 2018.
[30] Xu, Peiwen. A novel splicing mutation in the PKD1 gene causes autosomal dominant polycystic kidney disease in.... BMC MEDICAL GENETICS, 19, 2018.

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