Chunyan Jin

399 Hailing South Road
Taizhou, 225300, China

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 10 publications

Clinical application value of targeted amplicon sequencing technology in fetuses with uniparental disomy-related imprinting disorders: a multicenter study.

Clinical application value of targeted amplicon sequencing technology in fetuses with uniparental disomy-related imprinting disorders: a multicenter study.

Journal: Journal of translational medicine

Published: January 03, 2025

Study on the Clinical Value of Noninvasive Prenatal Testing in Screening the Chromosomal Abnormalities of the Fetus in the Elderly Pregnant Women.

Study on the Clinical Value of Noninvasive Prenatal Testing in Screening the Chromosomal Abnormalities of the Fetus in the Elderly Pregnant Women.

Journal: Computational and mathematical methods in medicine

Published: August 16, 2022

Exosomal miR-543 derived from umbilical cord mesenchymal stem cells ameliorates endometrial fibrosis in intrauterine adhesion via downregulating N-cadherin.

Exosomal miR-543 derived from umbilical cord mesenchymal stem cells ameliorates endometrial fibrosis in intrauterine adhesion via downregulating N-cadherin.

Journal: Placenta

Published: July 15, 2022

Mosaic trisomy 20: discrepancy between cyto-and molecular genetic technologies in prenatal diagnosis

Mosaic trisomy 20: discrepancy between cyto-and molecular genetic technologies in prenatal diagnosis

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

Published: July 10, 2022

Prenatal diagnosis by whole exome sequencing in a family with a novel TBR1 mutation causing intellectual disability.

Prenatal diagnosis by whole exome sequencing in a family with a novel TBR1 mutation causing intellectual disability.

Journal: Taiwanese journal of obstetrics & gynecology

Published: June 15, 2021

Identification of a novel TP63 mutation causing nonsyndromic cleft lip with or without cleft palate.

Identification of a novel TP63 mutation causing nonsyndromic cleft lip with or without cleft palate.

Journal: BMC medical genomics

Published: January 07, 2021

A prenatal diagnosis case of partial duplication 21q21.1-q21.2 with normal phenotype maternally inherited.

A prenatal diagnosis case of partial duplication 21q21.1-q21.2 with normal phenotype maternally inherited.

Journal: BMC medical genomics

Published: November 28, 2020

LncRNA-ATB Promotes the Tumorigenesis of Ovarian Cancer via Targeting miR-204-3p.

LncRNA-ATB Promotes the Tumorigenesis of Ovarian Cancer via Targeting miR-204-3p.

Journal: OncoTargets and therapy

Published: September 10, 2019

UCP2 Mitigates the Loss of Human Spermatozoa Motility by Promoting mROS Elimination.

UCP2 Mitigates the Loss of Human Spermatozoa Motility by Promoting mROS Elimination.

Journal: Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology

Published: January 23, 2018

Effects of Folpet, Captan, and Captafol on Human Aromatase in JEG-3 Cells.

Effects of Folpet, Captan, and Captafol on Human Aromatase in JEG-3 Cells.

Journal: Pharmacology

Published: June 02, 2017

Showing 1-10 of 10

Last Updated: 09/26/2026