Shun-ping Chang

Chang-hua, TNQ, Taiwan

Last Updated: 09/26/2026

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Found 38 publications

Non-Inversion Variants in Sporadic Hemophilia A Rarely Recur.

Non-Inversion Variants in Sporadic Hemophilia A Rarely Recur.

Journal: International journal of molecular sciences

Published: February 10, 2026

Genotype-Specific Postural Control Deficits in Hemophilia A: Insights from Center of Pressure Analysis Beyond Radiographic Arthropathy.

Genotype-Specific Postural Control Deficits in Hemophilia A: Insights from Center of Pressure Analysis Beyond Radiographic Arthropathy.

Journal: International journal of molecular sciences

Published: January 19, 2026

Molecular cytogenetic characterization of a de novo small supernumerary marker chromosome detected by amniocentesis and derived from the acrocentric chromosome 14/22.

Molecular cytogenetic characterization of a de novo small supernumerary marker chromosome detected by amniocentesis and derived from the acrocentric chromosome 14/22.

Journal: Taiwanese journal of obstetrics & gynecology

Published: November 13, 2025

Hidden translocation between 15qter and 18qter impressed during cycles of preimplantation genetic testing using linkage analyses and chromosome microarray subsequently verified by fluorescence in situ hybridization.

Hidden translocation between 15qter and 18qter impressed during cycles of preimplantation genetic testing using linkage analyses and chromosome microarray subsequently verified by fluorescence in situ hybridization.

Journal: Taiwanese journal of obstetrics & gynecology

Published: May 17, 2025

Utility of long-read sequencing to delineate a rare large deletion of beta-globin gene which escaped Sanger sequencing at prenatal diagnosis in a family clustered with hereditary persistence of fetal hemoglobin.

Utility of long-read sequencing to delineate a rare large deletion of beta-globin gene which escaped Sanger sequencing at prenatal diagnosis in a family clustered with hereditary persistence of fetal hemoglobin.

Journal: Taiwanese journal of obstetrics & gynecology

Published: April 14, 2025

Noninversion Variants in Sporadic Hemophilia A Originate Mostly from Females.

Noninversion Variants in Sporadic Hemophilia A Originate Mostly from Females.

Journal: International journal of molecular sciences

Published: December 13, 2024

Genetic investigations of autosomal recessive inherited ichthyosis impressed by fetal ultrasound: Exome sequencing and haplotype linkage analysis.

Genetic investigations of autosomal recessive inherited ichthyosis impressed by fetal ultrasound: Exome sequencing and haplotype linkage analysis.

Journal: Taiwanese journal of obstetrics & gynecology

Published: March 01, 2024

De Novo Noninversion Variants Implicated in Sporadic Hemophilia A: A Variant Origin and Timing Study.

De Novo Noninversion Variants Implicated in Sporadic Hemophilia A: A Variant Origin and Timing Study.

Journal: International journal of molecular sciences

Published: November 15, 2023

Low-level mosaic trisomy 13 at amniocentesis in a pregnancy associated with a positive NIPT result suspicious of trisomy 13, a CVS result of mosaic trisomy 13, cytogenetic discrepancy in various tissues and a favorable fetal outcome.

Low-level mosaic trisomy 13 at amniocentesis in a pregnancy associated with a positive NIPT result suspicious of trisomy 13, a CVS result of mosaic trisomy 13, cytogenetic discrepancy in various tissues and a favorable fetal outcome.

Journal: Taiwanese journal of obstetrics & gynecology

Published: May 03, 2023

Skewed X-Chromosome Inactivation and Parental Gonadal Mosaicism Are Implicated in X-Linked Recessive Female Hemophilia Patients.

Skewed X-Chromosome Inactivation and Parental Gonadal Mosaicism Are Implicated in X-Linked Recessive Female Hemophilia Patients.

Journal: Diagnostics (Basel, Switzerland)

Published: August 11, 2022

Origin and timing of de novo variants implicated in type 2 von Willebrand disease.

Origin and timing of de novo variants implicated in type 2 von Willebrand disease.

Journal: Journal of cellular and molecular medicine

Published: June 23, 2022

Prenatal diagnosis and molecular cytogenetic characterization of a familial small supernumerary marker chromosome derived from the acrocentric chromosome 14/22.

Prenatal diagnosis and molecular cytogenetic characterization of a familial small supernumerary marker chromosome derived from the acrocentric chromosome 14/22.

Journal: Taiwanese journal of obstetrics & gynecology

Published: January 13, 2022

Showing 1-12 of 38

Last Updated: 09/26/2026