Wen-hsiang B. Lin

Nangang Business Park
TPQ 11503, Taiwan

Last Updated: 09/26/2026

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Found 24 publications

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

Double body effect induced by integrating proprioceptive-vestibular and visual information.

Double body effect induced by integrating proprioceptive-vestibular and visual information.

Journal: iScience

Published: May 14, 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

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

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

Benefits and risks of low molecular weight heparin use on reproductive outcomes: A retrospective cohort study.

Benefits and risks of low molecular weight heparin use on reproductive outcomes: A retrospective cohort study.

Journal: Taiwanese journal of obstetrics & gynecology

Published: May 18, 2022

Polyhydramnios as a sole ultrasonographic finding for detecting fetal hemolytic anemia caused by anti-c alloimmunization.

Polyhydramnios as a sole ultrasonographic finding for detecting fetal hemolytic anemia caused by anti-c alloimmunization.

Journal: Taiwanese journal of obstetrics & gynecology

Published: April 29, 2022

Proposal for Practical Approach in Prenatal Diagnosis of Beckwith-Wiedemann Syndrome and Review of the Literature.

Proposal for Practical Approach in Prenatal Diagnosis of Beckwith-Wiedemann Syndrome and Review of the Literature.

Journal: Diagnostics (Basel, Switzerland)

Published: March 22, 2022

Prenatal Diagnosis of True Fetal Mosaicism with Small Supernumerary Marker Chromosome Derived from Chromosome 16 by Funipuncture and Molecular Cytogenetics Including Chromosome Microarray.

Prenatal Diagnosis of True Fetal Mosaicism with Small Supernumerary Marker Chromosome Derived from Chromosome 16 by Funipuncture and Molecular Cytogenetics Including Chromosome Microarray.

Journal: Diagnostics (Basel, Switzerland)

Published: July 14, 2021

Comparison of Genetic Profiling between Primary Tumor and Circulating Tumor Cells Captured by Microfluidics in Epithelial Ovarian Cancer: Tumor Heterogeneity or Allele Dropout?

Comparison of Genetic Profiling between Primary Tumor and Circulating Tumor Cells Captured by Microfluidics in Epithelial Ovarian Cancer: Tumor Heterogeneity or Allele Dropout?

Journal: Diagnostics (Basel, Switzerland)

Published: May 27, 2021

Experiential ownership and body ownership are different phenomena.

Experiential ownership and body ownership are different phenomena.

Journal: Scientific reports

Published: November 03, 2020

Whole Exome Sequencing with Comprehensive Gene Set Analysis Identified a Biparental-Origin Homozygous c.509G>A Mutation in PPIB Gene Clustered in Two Taiwanese Families Exhibiting Fetal Skeletal Dysplasia during Prenatal Ultrasound.

Whole Exome Sequencing with Comprehensive Gene Set Analysis Identified a Biparental-Origin Homozygous c.509G>A Mutation in PPIB Gene Clustered in Two Taiwanese Families Exhibiting Fetal Skeletal Dysplasia during Prenatal Ultrasound.

Journal: Diagnostics (Basel, Switzerland)

Published: March 30, 2020

Showing 1-12 of 24

Last Updated: 09/26/2026