T. Jiang

发表

Clinical Application of LC–MS/MS in the Follow-Up for Treatment of Children with Methylmalonic Aciduria

Yun Sun, Yanyun Wang, T. Jiang, 2019, Advances in Therapy.

Very Long-Chain Acyl-Coenzyme A Dehydrogenase Deficiency

Wei Cheng, Yun Sun, Yanyun Wang, 2014 .

Apert Syndrome With FGFR2 758 C > G Mutation: A Chinese Case Report

Yun Sun, Yanyun Wang, T. Jiang, 2018, Front. Genet..

Neonatal Screening and Genotype-Phenotype Correlation of 21-Hydroxylase Deficiency in the Chinese Population

Yun Sun, Yanyun Wang, T. Jiang, 2021, Frontiers in Genetics.

Clinical features and genotyping of patients with primary carnitine deficiency identified by newborn screening

Yun Sun, Yanyun Wang, T. Jiang, 2017, Journal of pediatric endocrinology & metabolism : JPEM.

Relationship between amniotic fluid metabolic profile with fetal gender, maternal age, and gestational week

Zhengfeng Xu, Yun Sun, P. Hu, 2021, BMC Pregnancy and Childbirth.

Perinatal outcomes following cell‐free DNA screening in >32 000 women: Clinical follow‐up data from a single tertiary center

Zhengfeng Xu, P. Hu, T. Jiang, 2018, Prenatal diagnosis.

Identification and characterization of a novel 43-bp deletion mutation of the ATP7B gene in a Chinese patient with Wilson’s disease: a case report

Gang Liu, Zhengfeng Xu, Yun Sun, 2018, BMC Medical Genetics.

Carrier screening and prenatal diagnosis for Spinal Muscular Atrophy in 13 069 Chinese pregnant women.

Zhengfeng Xu, Yun Sun, P. Hu, 2020, The Journal of molecular diagnostics : JMD.

Noninvasive prenatal diagnosis of 21-Hydroxylase deficiency using target capture sequencing of maternal plasma DNA

Xin Yi, Ping Hu, Wei Wang, 2017, Scientific Reports.

Molecular analysis of the CYP21A2 gene in Chinese patients with steroid 21-hydroxylase deficiency.

Zhengfeng Xu, Yun Sun, Yulin Chen, 2014, Clinical biochemistry.

Noninvasive prenatal diagnosis for X-linked disease by maternal plasma sequencing in a family of Hemophilia B.

Hui Jiang, R. Sun, Zhengfeng Xu, 2017, Taiwanese journal of obstetrics & gynecology.

Significance of data analysis in the quality control of prenatal screening for Down syndrome.

Yun Sun, T. Jiang, D. Hong, 2018, Biomedical reports.

A Novel Whole Gene Deletion of BCKDHB by Alu-Mediated Non-allelic Recombination in a Chinese Patient With Maple Syrup Urine Disease

Gang Liu, Zhengfeng Xu, Yun Sun, 2018, Front. Genet..

Clinical application of whole‐genome low‐coverage next‐generation sequencing to detect and characterize balanced chromosomal translocations

Asan, Y. Wang, Y. Lin, 2017, Clinical genetics.

Clinical application of SNP array analysis in first‐trimester pregnancy loss: a prospective study

Y Wang, Y. Wang, J. Zhang, 2017, Clinical genetics.

Identification of one novel CHD7 mutation in a patient from China with atypical CHARGE syndrome.

Zhengfeng Xu, P. Hu, T. Jiang, 2015, Gene.

Functional Characterization of Argininosuccinate Lyase Gene Variants by Mini-Gene Splicing Assay

Yun Sun, Yanyun Wang, T. Jiang, 2019, Front. Genet..

Analysis of five cases of hypermethioninemia diagnosed by neonatal screening

Yun Sun, Yanyun Wang, T. Jiang, 2019, Journal of pediatric endocrinology & metabolism : JPEM.

[ASS1 mutation leading to citrullinemia I in a Chinese Han family].

Zhang-bin Yu, Zhengfeng Xu, Yun Sun, 2011, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Value of Phenylalanine in Amniotic Fluid Detected by MS/MS for Screening of ma ternal PKU in the Second-Trimester

Yun Sun, Yanyun Wang, T. Jiang, 2020 .

Haplotype-based approach for noninvasive prenatal diagnosis of congenital adrenal hyperplasia by maternal plasma DNA sequencing.

Yanyan Zhang, Hui Jiang, Xun Xu, 2014, Gene.

Early Second-Trimester Peptidomic Identification of Serum Peptides for Potential Prediction of Gestational Diabetes Mellitus

Chun Zhao, Lingfeng Yin, H. Ding, 2018, Cellular Physiology and Biochemistry.