Xiang-yi H. Jing

107 Yanjiang West Road
Guangzhou, 510080, China

Last Updated: 09/26/2026

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Found 34 publications

Prenatal and molecular characteristics of 23 cases with Silver-Russell syndrome.

Prenatal and molecular characteristics of 23 cases with Silver-Russell syndrome.

Journal: Fetal diagnosis and therapy

Published: March 20, 2026

Genetic Investigation of Fetal Left-Right Laterality Defects Identified in the Second Trimester of Pregnancy.

Genetic Investigation of Fetal Left-Right Laterality Defects Identified in the Second Trimester of Pregnancy.

Journal: Prenatal diagnosis

Published: March 03, 2026

Prenatal Diagnosis of Neurofibromatosis Type 1: No Specific Prenatal Features Observed in Sporadic Fetal Presentations.

Prenatal Diagnosis of Neurofibromatosis Type 1: No Specific Prenatal Features Observed in Sporadic Fetal Presentations.

Journal: Prenatal diagnosis

Published: December 04, 2025

Fetal Isolated Unilateral Multicystic Dysplastic Kidney Identified on Second Trimester Ultrasound: Genetic Investigation Results at a Single Referral Center.

Fetal Isolated Unilateral Multicystic Dysplastic Kidney Identified on Second Trimester Ultrasound: Genetic Investigation Results at a Single Referral Center.

Journal: Prenatal diagnosis

Published: August 09, 2025

Isolated Hypospadias Identified on Fetal Ultrasound: Genetic Investigation Results at a Single Referral Center.

Isolated Hypospadias Identified on Fetal Ultrasound: Genetic Investigation Results at a Single Referral Center.

Journal: Fetal diagnosis and therapy

Published: July 17, 2025

Prenatal Diagnosis of Rubinstein-Taybi Syndrome-Reporting Twelve Cases of a Rare Disease.

Prenatal Diagnosis of Rubinstein-Taybi Syndrome-Reporting Twelve Cases of a Rare Disease.

Journal: Prenatal diagnosis

Published: July 09, 2025

Prenatal Diagnosis of KBG Syndrome: Phenotypic and Genotypic Features of 12 Fetal Cases With the Disorder.

Prenatal Diagnosis of KBG Syndrome: Phenotypic and Genotypic Features of 12 Fetal Cases With the Disorder.

Journal: Prenatal diagnosis

Published: November 04, 2024

Invasive genetic testing for isolated increased nuchal translucency of 3.0-3.4 mm: Results from cohort analysis with 604 fetuses.

Invasive genetic testing for isolated increased nuchal translucency of 3.0-3.4 mm: Results from cohort analysis with 604 fetuses.

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

Published: June 30, 2024

A Large Stomach on Fetal Ultrasound: More than Intestinal Obstruction.

A Large Stomach on Fetal Ultrasound: More than Intestinal Obstruction.

Journal: Journal of medical ultrasound

Published: April 03, 2024

Prenatal phenotype of 10p15.3 microdeletion syndrome: A series of five cases.

Prenatal phenotype of 10p15.3 microdeletion syndrome: A series of five cases.

Journal: Taiwanese journal of obstetrics & gynecology

Published: January 13, 2024

Improved outcomes in patients with prenatally detected 22q11.2 deletion syndrome.

Improved outcomes in patients with prenatally detected 22q11.2 deletion syndrome.

Journal: American journal of obstetrics and gynecology

Published: September 19, 2023

Fetal phenotype of Cornelia de Lange syndrome with a molecular confirmation.

Fetal phenotype of Cornelia de Lange syndrome with a molecular confirmation.

Journal: European journal of obstetrics, gynecology, and reproductive biology

Published: February 21, 2023

Showing 1-12 of 34

Last Updated: 09/26/2026