Fengxiang Wei

Balanced translocation t(3;18)(p13;q22.3) and points mutation in the ZNF407 gene detected in patients with both moderate non-syndromic intellectual disability and autism.

D. Tang, Shouqiang Zhong, Ya-Nan Zhang, 2013, Biochimica et biophysica acta.

Genotyping of five chinese patients with 17alpha-hydroxylase deficiency diagnosed through high-performance liquid chromatography serum adrenal profile: identification of two novel CYP17 mutations.

Fengxiang Wei, Ji-Qing Wei, Ji-Lu Wei, 2006, The Journal of clinical endocrinology and metabolism.

First report of a Chinese patient carrying Hb Ty Gard: A case report

Fengxiang Wei, Jian Ran, Yu-Heng Pei, 2022, Medicine.

Concomitant 1 q 42 . 13-q 44 Duplication and 14 q 32 . 33 Deletion : A Case Report and Review of Literature

Brittany Grommisch, Fang Xu, Peining Li, 2017 .

Novel Mutation of SYNGAP1 Associated with Autosomal Dominant Mental Retardation 5 in a Chinese Patient

L. Du, Fengxiang Wei, Wei Li, 2018, Fetal and pediatric pathology.

Two Novel Pathogenic Variants of TJP2 Gene and the Underlying Molecular Mechanisms in Progressive Familial Intrahepatic Cholestasis Type 4 Patients

L. Luo, Xiaofen Ma, Shengmei Zhou, 2021, Frontiers in Cell and Developmental Biology.

Prenatal diagnosis and pregnancy determination of sex chromosome aneuploidy screened by non-invasive prenatal testing from 52,453 unselected singleton pregnancies: a retrospective analysis of 4-year experience

Fengxiang Wei, Xiaojing Luo, Gao-Chi Li, 2020 .

Non-invasive preeclampsia prediction using plasma cell-free RNA signatures.

Huiyan Jiang, Haixi Sun, Jie Li, 2023, American journal of obstetrics and gynecology.