Fan Jiang

Guangzhou, China

Last Updated: 09/26/2026

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Found 51 publications

Fetal Interrupted Aortic Arch and Unilateral Duplex Kidney Identified by Second Trimester Ultrasound Prompting Genetic Diagnosis of Neonatal Sclerosing Cholangitis.

Fetal Interrupted Aortic Arch and Unilateral Duplex Kidney Identified by Second Trimester Ultrasound Prompting Genetic Diagnosis of Neonatal Sclerosing Cholangitis.

Journal: Prenatal diagnosis

Published: April 02, 2026

Clinically Significant Genetic Results in Fetuses With Isolated Horseshoe Kidney.

Clinically Significant Genetic Results in Fetuses With Isolated Horseshoe Kidney.

Journal: Prenatal diagnosis

Published: October 26, 2025

A Novel Large Deletion Including the Major Regulatory Element Compounded with SEA Deletion Causing Hydrops-Fetalis-Syndrome.

A Novel Large Deletion Including the Major Regulatory Element Compounded with SEA Deletion Causing Hydrops-Fetalis-Syndrome.

Journal: Hemoglobin

Published: June 10, 2025

First Reported Case of Hemoglobin H Disease Caused by the Rare α-Globin Gene Mutation (HBA2 c.244delT) in a Chinese Family.

First Reported Case of Hemoglobin H Disease Caused by the Rare α-Globin Gene Mutation (HBA2 c.244delT) in a Chinese Family.

Journal: Hemoglobin

Published: January 03, 2025

An unusual transfusion-dependent hemoglobin H disease caused by a novel complex inverted duplication involving the α-globin regulatory elements and α-thalassemia--SEA deletion.

An unusual transfusion-dependent hemoglobin H disease caused by a novel complex inverted duplication involving the α-globin regulatory elements and α-thalassemia--SEA deletion.

Journal: Annals of hematology

Published: November 05, 2024

Identification of a Novel 16.8Kb Deletion of the α-Globin Gene Cluster by Third-Generation Sequencing.

Identification of a Novel 16.8Kb Deletion of the α-Globin Gene Cluster by Third-Generation Sequencing.

Journal: Hemoglobin

Published: July 15, 2024

A 6-Year Follow-up of a Chinese Child with Homozygous β0-Thalaasemia and a Heterozygous KLF1 Mutation.

A 6-Year Follow-up of a Chinese Child with Homozygous β0-Thalaasemia and a Heterozygous KLF1 Mutation.

Journal: Hemoglobin

Published: February 05, 2024

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

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

Journal: Hemoglobin

Published: October 09, 2023

Utilization of multiple genetic methods for prenatal diagnosis of rare thalassemia variants.

Utilization of multiple genetic methods for prenatal diagnosis of rare thalassemia variants.

Journal: Frontiers in genetics

Published: April 18, 2023

Identification of a Novel Mutation in the 3' Untranslated Region of the β-Globin Gene (HBB:c.*132C>G) in a Chinese Family.

Identification of a Novel Mutation in the 3' Untranslated Region of the β-Globin Gene (HBB:c.*132C>G) in a Chinese Family.

Journal: Hemoglobin

Published: March 06, 2023

Application of real-time PCR-based multicolor melting curve with automatic analysis system in pregestational and prenatal thalassemia diagnoses.

Application of real-time PCR-based multicolor melting curve with automatic analysis system in pregestational and prenatal thalassemia diagnoses.

Journal: Annals of human genetics

Published: February 08, 2023

Molecular Epidemiological Characteristics and Differential Diagnosis of Common δβ-Thalassemia/HPFH

Molecular Epidemiological Characteristics and Differential Diagnosis of Common δβ-Thalassemia/HPFH

Journal: Zhongguo shi yan xue ye xue za zhi

Published: August 18, 2022

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Last Updated: 09/26/2026