Huanzheng Li

6PUBLICATIONS
6CO-AUTHORS
Foetal development and medicineGene expression (incl. microarray and other genome-wide approaches)Gene mappingInfant and child healthStructural properties of condensed matter
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Publications (6)

|Oct 15, 2026
Prenatal Diagnosis and Postnatal Follow-Up of 19 Fetuses With 16p13.11 Microduplication in a Cohort of 12,038 Pregnancies From South Zhejiang.

|Jun 09, 2026
Differential Transcriptome Analysis of Intrauterine UPD6pat Fetuses With Distinct Phenotypes.

|Feb 24, 2025
Saliva Sample-Based Non-Invasive Carrier Screening for Spinal Muscular Atrophy, Hereditary Hearing Loss, and Thalassemia in 13,926 Women of Reproductive Age From South Zhejiang.

Chenyang Xu, Yanbao Xiang, Xiaoling Lin

|Aug 08, 2023
PLPPR4 haploinsufficiency causes neurodevelopmental disorders by disrupting synaptic plasticity via mTOR signalling.

Huanzheng Li, Qian Zhang, Ru Wan

|Feb 27, 2021
Mutation analysis and prenatal diagnosis of a family with congenital contractural arachnodactyly.

Lin Hu, Huanzheng Li, Guang Sun

|Oct 23, 2020
Next-generation sequencing identifies rare pathogenic and novel candidate variants in a cohort of Chinese patients with syndromic or nonsyndromic hearing loss.

Yan-Bao Xiang, Chen-Yang Xu, Yun-Zhi Xu

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Frequent Collaborators

2 joint publications

Shaohua Tang

1 joint publications

Lin Hu

1 joint publications

Chenyang Xu

1 joint publications

Xiaohua Tang