Li Du

Guangzhou, China

Last Updated: 09/26/2026

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Found 30 publications

Prevention and control of thalassemia in Guangdong Province, Southern China: insights from an 11-year retrospective study.

Prevention and control of thalassemia in Guangdong Province, Southern China: insights from an 11-year retrospective study.

Journal: Annals of medicine

Published: August 22, 2025

A one-base therapeutic insertion in the HBG2 distal promoter reactivates γ-globin expression.

A one-base therapeutic insertion in the HBG2 distal promoter reactivates γ-globin expression.

Journal: Experimental hematology & oncology

Published: February 11, 2025

ALG8-CDG: advances in molecular and prenatal phenotyping facilitate prenatal diagnosis and genetic counseling.

ALG8-CDG: advances in molecular and prenatal phenotyping facilitate prenatal diagnosis and genetic counseling.

Journal: QJM : monthly journal of the Association of Physicians

Published: November 20, 2024

Exome sequencing for nonimmune hydrops fetalis and clinical utility of data reanalysis.

Exome sequencing for nonimmune hydrops fetalis and clinical utility of data reanalysis.

Journal: QJM : monthly journal of the Association of Physicians

Published: August 06, 2024

Two novel deletion mutations in β-globin gene cause β-thalassemia trait in two Chinese families.

Two novel deletion mutations in β-globin gene cause β-thalassemia trait in two Chinese families.

Journal: Human genomics

Published: September 11, 2023

Abnormal hemoglobin anti-Lepore Hong Kong compound with β0-thalassemia ameliorate thalassemia severity when co-inherited with α-thalassemia.

Abnormal hemoglobin anti-Lepore Hong Kong compound with β0-thalassemia ameliorate thalassemia severity when co-inherited with α-thalassemia.

Journal: Scientific reports

Published: May 10, 2023

Hb Chapel Hill or Alpha2 74(EF3) Asp>Gly, a mildly unstable variant found in a Chinese family.

Hb Chapel Hill or Alpha2 74(EF3) Asp>Gly, a mildly unstable variant found in a Chinese family.

Journal: Hematology (Amsterdam, Netherlands)

Published: March 20, 2023

Hb Q-Thailand heterozygosity unlinked with the (-α4.2/) α+-thalassemia deletion allele identified by long-read SMRT sequencing: hematological and molecular analyses.

Hb Q-Thailand heterozygosity unlinked with the (-α4.2/) α+-thalassemia deletion allele identified by long-read SMRT sequencing: hematological and molecular analyses.

Journal: Hematology (Amsterdam, Netherlands)

Published: March 03, 2023

A Novel 5 kb Deletion in the β-Globin Gene Cluster Identified in a Chinese Patient.

A Novel 5 kb Deletion in the β-Globin Gene Cluster Identified in a Chinese Patient.

Journal: Hemoglobin

Published: October 10, 2022

Identification of four novel large deletions and complex variants in the α-globin locus in Chinese population.

Identification of four novel large deletions and complex variants in the α-globin locus in Chinese population.

Journal: Human genomics

Published: October 07, 2022

First study to describe a novel HbA2: c.400A > C mutation and Hb Dongguan heterozygote in two unrelated Chinese families.

First study to describe a novel HbA2: c.400A > C mutation and Hb Dongguan heterozygote in two unrelated Chinese families.

Journal: Hematology (Amsterdam, Netherlands)

Published: August 08, 2022

The -α3.7III subtype of α+-thalassemia was identified in China.

The -α3.7III subtype of α+-thalassemia was identified in China.

Journal: Hematology (Amsterdam, Netherlands)

Published: August 02, 2022

Showing 1-12 of 30

Last Updated: 09/26/2026