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Profile of Dr. Zi-Jiang Chen

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摘要 Dr. Chen received her bachelor-equivelent medical education at School of Medicine Shandong University (previously the Shandong Medical College), and got her MD–Ph D in1989 majoring in Obstetrics and Gynecology. As the youngest professor in the school’s history, Dr. Chen joined the faculty of School of Medicine Shandong University.
出处 《Science China(Life Sciences)》 SCIE CAS CSCD 2020年第6期845-848,共4页 中国科学（生命科学英文版）
关键词 NAT Profile of Dr Zi-Jiang Chen
分类号 R192.3 [医药卫生—卫生事业管理]
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  • 1Morton CC, Nance WE. Newborn heating screening-a silent revolu- tion. N Engl J Med, 2006, 354:2151-2164.
  • 2Mujezinovic F, Alfirevic Z. Procedure-related complications of am- niocentesis and chorionic villous sampling: a systematic review. Ob- stet Gynecol, 2007, 110:687-694.
  • 3Akolekar R, Beta J, Picciarelli G, Ogilvie C, D'Antonio F. Proce- dure-related risk of miscarriage following amniocentesis and chori- onic villus sampling: a systematic review and meta-analysis. Ultra- sound Obstet Gynecol, 2015, 45:16-26.
  • 4Liss J, Mirecka A, Kitowska K, Lukaszuk K. Preimplantaion genetic diagnosis of hearing loss with 35delG mutation in GJB2 gene - pre- liminary report. Otolaryngol Pol, 2011, 65:443-446.
  • 5Wu CC, Lin SY, Su YN, Fang MY, Chen SU, Hsu CJ. Preimplanta- tion genetic diagnosis (embryo screening) for enlarged vestibular aq- ueduct due to SLC26A4 mutation. Audiol Neurootol, 2010, 15: 311-317.
  • 6Moutou C GV, Coonen E, De Rycke M, Kokkali G, Renwick P, SenGupta SB, Vesela K, Traeger-Synodinos J. ESHRE PGD Consor- tium data collection XII: cycles from January to December 2009 with pregnancy follow-up to October 2010. Hum Reprod, 2014, 29: 880-903.
  • 7Altarescu G, Eldar-Geva T, Brooks B, Zylber-Haran E, Varshaver I, Margalioth EJ, Levy-Lahad E, Renbaum P. Preimplantation genetic diagnosis (PGD) for nonsyndromic deafness by polar body and blas- tomere biopsy. J Assist Reprod Genet, 2009, 26:391-397.
  • 8Meng M, Li XC, Ge H J, Chen F, Han MY, Zhang YY, Kang DY, Xie WW, Gao ZY, Pan XY, Dai P, Chi FL, Chen SP, Liu P, Zhang CL, Cao JJ, Jiang H, Xu X, Wang W, Duan T. Noninvasive prenatal testing for autosomal recessive conditions by maternal plasma se- quencing in a case of congenital deafness. Genet Med, 2014, 16: 972-976.
  • 9Huang LH, Han DM, Guo Y, Liu S, Cui XY, Mo LY, Qi B, Cai ZH, Liu H, En H, Guo LS. Audiological characteristics of infants with abnormal transient evoked otoacoustic emission and normal auditory brainstem response. Biosci Trends, 2008, 2:211-215.
  • 10Ji YB, Han DY, Lan L, Wang DY, Zong L, Zhao FF, Liu Q, Bene- dict-Alderfer C, Zheng QY, Wang QJ. Molecular epidemiological analysis of mitochondrial DNAI2SrRNA A1555G, GJB2, and SLC26A4 mutations in sporadic outpatients with nonsyndromic sen- sorineural hearing loss in China. Acta Otolaryngol, 2011, 131: 124-129.

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Science China(Life Sciences)
2020年 第6期

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