Chunxin Chang

910 Hengshan Road
Hengshan, China

Last Updated: 09/26/2026

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Found 11 publications

Universal noninvasive prenatal diagnosis for monogenic disorders using cell-free plasma DNA.

Universal noninvasive prenatal diagnosis for monogenic disorders using cell-free plasma DNA.

Journal: Genome medicine

Published: November 26, 2024

A Novel and Comprehensive Whole-Genome Sequencing-Based Preimplantation Genetic Testing Approach for Different Genetic Conditions.

A Novel and Comprehensive Whole-Genome Sequencing-Based Preimplantation Genetic Testing Approach for Different Genetic Conditions.

Journal: The Journal of molecular diagnostics : JMD

Published: October 11, 2024

Noninvasive preimplantation genetic testing for aneuploidy using blastocyst spent culture medium may serve as a backup of trophectoderm biopsy in conventional preimplantation genetic testing.

Noninvasive preimplantation genetic testing for aneuploidy using blastocyst spent culture medium may serve as a backup of trophectoderm biopsy in conventional preimplantation genetic testing.

Journal: BMC medical genomics

Published: September 19, 2024

Genetic analysis of 25 Chinese pedigrees with neurofibromatosis type 1 and genotype-phenotype study from an extended cohort.

Genetic analysis of 25 Chinese pedigrees with neurofibromatosis type 1 and genotype-phenotype study from an extended cohort.

Journal: Orphanet journal of rare diseases

Published: September 02, 2024

Associations between exposure to pesticides mixture and semen quality among the non-occupationally exposed males: Four statistical models.

Associations between exposure to pesticides mixture and semen quality among the non-occupationally exposed males: Four statistical models.

Journal: Environmental research

Published: February 04, 2024

An Effective and Universal Long-Read Sequencing-Based Approach for SMN1 2 + 0 Carrier Screening through Family Trio Analysis.

An Effective and Universal Long-Read Sequencing-Based Approach for SMN1 2 + 0 Carrier Screening through Family Trio Analysis.

Journal: Clinical chemistry

Published: July 05, 2023

Comprehensive Analysis of Spinal Muscular Atrophy: SMN1 Copy Number, Intragenic Mutation, and 2 + 0 Carrier Analysis by Third-Generation Sequencing.

Comprehensive Analysis of Spinal Muscular Atrophy: SMN1 Copy Number, Intragenic Mutation, and 2 + 0 Carrier Analysis by Third-Generation Sequencing.

Journal: The Journal of molecular diagnostics : JMD

Published: March 04, 2022

Prenatal diagnosis of spinal muscular atrophy using multiple ligation-dependent probe amplification

Prenatal diagnosis of spinal muscular atrophy using multiple ligation-dependent probe amplification

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: March 22, 2021

Expanding the Scope of Non-invasive Prenatal Testing to Detect Fetal Chromosomal Copy Number Variations.

Expanding the Scope of Non-invasive Prenatal Testing to Detect Fetal Chromosomal Copy Number Variations.

Journal: Frontiers in molecular biosciences

Published: January 04, 2021

Comprehensive copy number analysis of Y chromosome-linked loci for detection of structural variations and diagnosis of male infertility.

Comprehensive copy number analysis of Y chromosome-linked loci for detection of structural variations and diagnosis of male infertility.

Journal: Journal of human genetics

Published: December 11, 2020

Preimplantation Genetic Testing for a Chinese Family With X-Linked Lymphoproliferative Syndrome Type 1.

Preimplantation Genetic Testing for a Chinese Family With X-Linked Lymphoproliferative Syndrome Type 1.

Journal: Frontiers in genetics

Published: April 09, 2020

Showing 1-11 of 11

Last Updated: 09/26/2026