Zhi-qing Xiao

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

Journal: Prenatal diagnosis

Published: December 04, 2025

Clinically Significant Genetic Results in Fetuses With Isolated Horseshoe Kidney.

Journal: Prenatal diagnosis

Published: October 26, 2025

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.

Journal: Fetal diagnosis and therapy

Published: July 17, 2025

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

Journal: Prenatal diagnosis

Published: July 09, 2025

Fetal exome sequencing for increased nuchal translucency: how we do it.

Journal: American journal of obstetrics and gynecology

Published: May 18, 2025

Genetic Investigation of Fetuses With Isolated Unilateral Renal Agenesis Identified on Second Trimester Ultrasound: A Single Referral Center Experience.

Journal: Prenatal diagnosis

Published: May 15, 2025

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

Journal: Prenatal diagnosis

Published: November 04, 2024

Exome Sequencing in Fetuses With Bilateral Renal Agenesis Identified on Second Trimester Ultrasound: A Single Referral Center Experience.

Journal: Prenatal diagnosis

Published: August 21, 2024

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

Oligohydramnios and an empty bladder with normal renal morphology: Renal tubular dysgenesis is an important consideration in the prenatal setting.

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

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.

Clinically Significant Genetic Results in Fetuses With Isolated Horseshoe Kidney.

Clinically Significant Genetic Results in Fetuses With Isolated Horseshoe Kidney.

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.

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.

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.

Fetal exome sequencing for increased nuchal translucency: how we do it.

Fetal exome sequencing for increased nuchal translucency: how we do it.

Genetic Investigation of Fetuses With Isolated Unilateral Renal Agenesis Identified on Second Trimester Ultrasound: A Single Referral Center Experience.

Genetic Investigation of Fetuses With Isolated Unilateral Renal Agenesis Identified on Second Trimester Ultrasound: A Single Referral Center Experience.

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.

Exome Sequencing in Fetuses With Bilateral Renal Agenesis Identified on Second Trimester Ultrasound: A Single Referral Center Experience.

Exome Sequencing in Fetuses With Bilateral Renal Agenesis Identified on Second Trimester Ultrasound: A Single Referral Center Experience.

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.

Oligohydramnios and an empty bladder with normal renal morphology: Renal tubular dysgenesis is an important consideration in the prenatal setting.

Oligohydramnios and an empty bladder with normal renal morphology: Renal tubular dysgenesis is an important consideration in the prenatal setting.

β-Thalassemia Trait Caused by SUPT5H Defects: Another Case Report.

β-Thalassemia Trait Caused by SUPT5H Defects: Another Case Report.