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Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 5, 2018
[Genetic analysis and prenatal diagnosis for 25 Chinese pedigrees affected with congenital adrenal hyperplasia due to 21-hydroxylase deficiency]Chunyu Luo, Tao Jiang, Jingjing Zhang, et al.
Frontiers in Genetics|September 5, 2018
Prenatal Diagnosis of Recurrent Distal 1q21.1 Duplication in Three Fetuses With Ultrasound AnomaliesXiuqing Ji, Qiong Pan, Yan Wang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 1, 2017
[Prenatal diagnosis of two fetuses with chromosome 1p36 deletion syndrome]Xiuqing Ji, Huanran Hu, Yan Wang, et al.
Plos One|May 17, 2012
Modification of cyclic NGR tumor neovasculature-homing motif sequence to human plasminogen kringle 5 improves inhibition of tumor growthWeiwei Jiang, Guanghui Jin, Dingyuan Ma, et al.
Prenatal Diagnosis|July 3, 2018
Perinatal outcomes following cell-free DNA screening in >32 000 women: Clinical follow-up data from a single tertiary centerDong Liang, Ying Lin, Fengchang Qiao, et al.
Clinical Biochemistry|February 8, 2014
Molecular analysis of the CYP21A2 gene in Chinese patients with steroid 21-hydroxylase deficiencyDingyuan Ma, Yulin Chen, Yun Sun, et al.
Cellular & Molecular Immunology|September 5, 2009
Expression, purification and characterization of C-FADDYuan Chen, Dingyuan Ma, Qi-Lai Huang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|July 21, 2023
Evaluating the performance of four assays for carrier screening of spinal muscular atrophyJianxin Tan, Jingjing Zhang, Ruihong Sun, et al.
Biotechnology and Applied Biochemistry|January 3, 2008
A monoclonal-antibody-based ELISA for the detection of human FADD (Fas-associated death domain)Jianqiang Ye, Hongxia Shao, Dingyuan Ma, et al.
Molecular Cytogenetics|December 31, 2015
Analysis of chromosome 22q11 copy number variations by multiplex ligation-dependent probe amplification for prenatal diagnosis of congenital heart defectJingjing Zhang, Dingyuan Ma, Yan Wang, et al.
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