Lei Wang

发表

Value of amniotic fluid homocysteine assay in prenatal diagnosis of combined methylmalonic acidemia and homocystinuria, cobalamin C type

Xuefan Gu, L. Liang, Hong-guang Zhu, 2020, Orphanet Journal of Rare Diseases.

A novel mutation identified in PKHD1 by targeted exome sequencing: guiding prenatal diagnosis for an ARPKD family.

Wen-ting Jiang, X. Ji, Yan Xu, 2014, Gene.

Haplotype-based approach for noninvasive prenatal tests of Duchenne muscular dystrophy using cell-free fetal DNA in maternal plasma

Ping Liu, Hui Jiang, Wen-ting Jiang, 2015, Genetics in Medicine.

Prenatal diagnosis of Duchenne muscular dystrophy in 131 Chinese families with dystrophinopathy

Wen-ting Jiang, X. Ji, Yan Xu, 2017, Prenatal diagnosis.

Biochemical and genetic approaches to the prenatal diagnosis of propionic acidemia in 78 pregnancies

Xuefan Gu, L. Liang, Yongguo Yu, 2020, Orphanet Journal of Rare Diseases.

Prenatal Diagnosis of Isovaleric Acidemia From Amniotic Fluid Using Genetic and Biochemical Approaches

Xuefan Gu, L. Liang, Simon C. K. Ding, 2022, Frontiers in Genetics.

Prenatal Diagnosis of Glutaric Acidemia I Based on Amniotic Fluid Samples in 42 Families Using Genetic and Biochemical Approaches

Yan Xu, Xuefan Gu, L. Liang, 2020, Frontiers in Genetics.

Prenatal diagnosis of methylmalonic aciduria from amniotic fluid using genetic and biochemical approaches

X. Ji, Yan Xu, Yingwei Chen, 2019, Prenatal diagnosis.

Value of amniotic fluid homocysteine assay in prenatal diagnosis of combined methylmalonic acidemia and homocystinuria, cobalamin C type

Xuefan Gu, L. Liang, Hong-guang Zhu, 2020, Orphanet Journal of Rare Diseases.

Prognosis and outcome of intrauterine treatment of fetuses with critical congenital heart disease.

Kun Sun, Hong-guang Zhu, Lei Wang, 2023, Chinese medical journal.