Huanhuan Wang

Novel noncontiguous duplications identified with a comprehensive mutation analysis in the DMD gene by DMD gene-targeted sequencing.

X. Ji, Yan Xu, Yingwei Chen, 2018, Gene.

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

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

Noninvasive prenatal test of methylmalonic academia cblC type through targeted sequencing of cell-free DNA in maternal plasma

Zhiyu Peng, X. Ji, Xuefan Gu, 2018, bioRxiv.

Type II antithrombin deficiency caused by a novel missense mutation (p.Leu417Gln) in a Chinese family.

Yan-hui Jin, Lihong Yang, Qiyu Xu, 2020, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

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

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

Noninvasive prenatal diagnosis of cobalamin C (cblC) deficiency through target region sequencing of cell‐free DNA in maternal plasma

Zhiyu Peng, X. Ji, Xuefan Gu, 2019, Prenatal diagnosis.

A novel homozygous missense mutation (Met527Ile) in a consanguineous marriage family with inherited factor XII deficiency

Lihong Yang, Meina Liu, Miaomiao Lin, 2020, Hematology.

Genetic analysis of compound heterozygous pathogenic variants of the F11 gene in two Chinese patients with hereditary factor XI deficiency

Lihong Yang, Huanhuan Wang, Mingshan Wang, 2021, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.