Chih-ling Chen

TPQ, Taiwan

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 11 publications

Prenatal diagnosis of 9q34.3 microdeletion-associated Kleefstra syndrome in a pregnancy complicated by polyhydramnios: A case report and literature review.

Prenatal diagnosis of 9q34.3 microdeletion-associated Kleefstra syndrome in a pregnancy complicated by polyhydramnios: A case report and literature review.

Journal: Taiwanese journal of obstetrics & gynecology

Published: June 19, 2024

Neonatal Filaggrin Genetic Screening and Counseling to Prevent Atopic Dermatitis in High-Risk Infants.

Neonatal Filaggrin Genetic Screening and Counseling to Prevent Atopic Dermatitis in High-Risk Infants.

Journal: Dermatitis : contact, atopic, occupational, drug

Published: April 02, 2024

Ethnically unique disease burden and limitations of current expanded carrier screening panels.

Ethnically unique disease burden and limitations of current expanded carrier screening panels.

Journal: International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics

Published: March 23, 2023

Clinical outcomes of fetuses with chromosome 16 short arm copy number variants.

Clinical outcomes of fetuses with chromosome 16 short arm copy number variants.

Journal: Molecular genetics & genomic medicine

Published: January 24, 2023

Novel Compound Heterozygous Variants in TBCD Gene Associated with Infantile Neurodegenerative Encephalopathy.

Novel Compound Heterozygous Variants in TBCD Gene Associated with Infantile Neurodegenerative Encephalopathy.

Journal: Children (Basel, Switzerland)

Published: November 10, 2021

First report of a successful pregnancy by preimplantation genetic testing for Beckwith-Wiedemann syndrome.

First report of a successful pregnancy by preimplantation genetic testing for Beckwith-Wiedemann syndrome.

Journal: Taiwanese journal of obstetrics & gynecology

Published: November 20, 2020

Fragile X syndrome carrier screening in pregnant women in Chinese Han population.

Fragile X syndrome carrier screening in pregnant women in Chinese Han population.

Journal: Scientific reports

Published: January 29, 2019

Complication rates after chorionic villus sampling and midtrimester amniocentesis: A 7-year national registry study.

Complication rates after chorionic villus sampling and midtrimester amniocentesis: A 7-year national registry study.

Journal: Journal of the Formosan Medical Association = Taiwan yi zhi

Published: October 29, 2018

Prenatal diagnosis of paternal uniparental disomy for chromosome 14 using a single-nucleotide-polymorphism-based microarray analysis: A case report.

Prenatal diagnosis of paternal uniparental disomy for chromosome 14 using a single-nucleotide-polymorphism-based microarray analysis: A case report.

Journal: Journal of the Formosan Medical Association = Taiwan yi zhi

Published: September 10, 2018

Genome-wide association analysis identifies a GLUL haplotype for familial hepatitis B virus-related hepatocellular carcinoma.

Genome-wide association analysis identifies a GLUL haplotype for familial hepatitis B virus-related hepatocellular carcinoma.

Journal: Cancer

Published: March 22, 2017

Transcervical double-balloon catheter as an alternative and salvage method for medical termination of pregnancy in midtrimester.

Transcervical double-balloon catheter as an alternative and salvage method for medical termination of pregnancy in midtrimester.

Journal: Taiwanese journal of obstetrics & gynecology

Published: December 18, 2015

Showing 1-11 of 11

Last Updated: 09/26/2026