Haixia Zhang

Chengdu, China

Last Updated: 09/26/2026

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Found 8 publications

The first prenatal diagnosis of EMC10-Related neurodevelopmental disorder: Expanding the phenotypic and mutational spectra through a case and literature review.

The first prenatal diagnosis of EMC10-Related neurodevelopmental disorder: Expanding the phenotypic and mutational spectra through a case and literature review.

Journal: Taiwanese journal of obstetrics & gynecology

Published: March 05, 2026

Prenatal Phenotype of a Heterozygous de Novo Missense COL4A1 Variant in a Fetus With Pleural Effusion, Ascites, Increased Placental Thickness, Decreased Amniotic Fluid, and Cerebral Structural Malformations.

Prenatal Phenotype of a Heterozygous de Novo Missense COL4A1 Variant in a Fetus With Pleural Effusion, Ascites, Increased Placental Thickness, Decreased Amniotic Fluid, and Cerebral Structural Malformations.

Journal: Prenatal diagnosis

Published: January 12, 2026

Asian Screening Array and Next-Generation Sequencing Based Panels Applied to Preimplantation Genetic Testing for Monogenic Disorders Preclinical Workup in 294 Families: A Retrospective Analysis.

Asian Screening Array and Next-Generation Sequencing Based Panels Applied to Preimplantation Genetic Testing for Monogenic Disorders Preclinical Workup in 294 Families: A Retrospective Analysis.

Journal: Prenatal diagnosis

Published: January 30, 2024

Third-generation sequencing identified a novel complex variant in a patient with rare alpha-thalassemia.

Third-generation sequencing identified a novel complex variant in a patient with rare alpha-thalassemia.

Journal: BMC pediatrics

Published: November 12, 2022

Analysis of rare thalassemia genetic variants based on third-generation sequencing.

Analysis of rare thalassemia genetic variants based on third-generation sequencing.

Journal: Scientific reports

Published: February 16, 2022

A rare complex rearrangement in the β-globin gene cluster causing a novel homozygous G γ(A γδβ)0 -thalassemia.

A rare complex rearrangement in the β-globin gene cluster causing a novel homozygous G γ(A γδβ)0 -thalassemia.

Journal: American journal of hematology

Published: January 26, 2021

Prenatal diagnosis of genetic aberrations in fetuses with short femur detected by ultrasound: A prospective cohort study.

Prenatal diagnosis of genetic aberrations in fetuses with short femur detected by ultrasound: A prospective cohort study.

Journal: Prenatal diagnosis

Published: June 30, 2020

Preliminary study of protein changes in trisomy 21 fetus by proteomics analysis in amniocyte.

Preliminary study of protein changes in trisomy 21 fetus by proteomics analysis in amniocyte.

Journal: Prenatal diagnosis

Published: December 07, 2017

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Last Updated: 09/26/2026