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Molecular Neurobiology|May 20, 2024
Creatine Kinase-MM/Proto-oncogene Tyrosine-Protein Kinase Receptor as a Sensitive Indicator for Duchenne Muscular Dystrophy CarriersZhilei Zhang, Dongyang Hong, 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.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 18, 2025
Genetic results and clinical outcome of fetuses with cardiac rhabdomyoma including a novel mutation in TSC2 geneJie Gao, Yun Wu, Dingyuan Ma, et al.
Gene|April 29, 2014
Haplotype-based approach for noninvasive prenatal diagnosis of congenital adrenal hyperplasia by maternal plasma DNA sequencingDingyuan Ma, Huijuan Ge, Xuchao Li, et al.
Taiwanese Journal of Obstetrics & Gynecology|October 18, 2017
Noninvasive prenatal diagnosis for X-linked disease by maternal plasma sequencing in a family of Hemophilia BPing Hu, Fengchang Qiao, Yuan Yuan, et al.
Scientific Reports|August 9, 2017
Noninvasive prenatal diagnosis of 21-Hydroxylase deficiency using target capture sequencing of maternal plasma DNADingyuan Ma, Yuan Yuan, Chunyu Luo, et al.
American Journal of Obstetrics and Gynecology|November 13, 2017
Prenatal chromosomal microarray analysis in fetuses with congenital heart disease: a prospective cohort studyYan Wang, Li Cao, Dong Liang, et al.
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