Lihong Zheng

Nanning, China

Last Updated: 09/26/2026

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Found 19 publications

Resolving diagnostic complexity: long-read sequencing unmasks a Hong Kongαα/‒α4.2 genotype mimicking a heterozygous ‒α3.7 deletion on multiplex ligation-dependent probe amplification.

Resolving diagnostic complexity: long-read sequencing unmasks a Hong Kongαα/‒α4.2 genotype mimicking a heterozygous ‒α3.7 deletion on multiplex ligation-dependent probe amplification.

Journal: Laboratory medicine

Published: August 10, 2026

Characterization of a novel α-thalassemia deletion (Dongxing deletion; --DX) by CNV-seq in a Chinese female with Hb H disease: a case report.

Characterization of a novel α-thalassemia deletion (Dongxing deletion; --DX) by CNV-seq in a Chinese female with Hb H disease: a case report.

Journal: Hematology (Amsterdam, Netherlands)

Published: June 19, 2026

Hb Baise (HBA2: C.153_154insGACCTG): An Unexpectedly Discovered Novel Variant in Glycated Hemoglobin Testing.

Hb Baise (HBA2: C.153_154insGACCTG): An Unexpectedly Discovered Novel Variant in Glycated Hemoglobin Testing.

Journal: Hemoglobin

Published: May 13, 2026

A Case of Hb Quong Sze Co-Inherited Thai Deletion Resulting in Falsely Elevated HbA1c Values.

A Case of Hb Quong Sze Co-Inherited Thai Deletion Resulting in Falsely Elevated HbA1c Values.

Journal: Clinical laboratory

Published: April 07, 2026

High prevalence of Hb Q-Thailand not in cis with the -α4.2 deletion: genotypes, phenotypes, and implications in the cenxi population of southern China.

High prevalence of Hb Q-Thailand not in cis with the -α4.2 deletion: genotypes, phenotypes, and implications in the cenxi population of southern China.

Journal: Frontiers in genetics

Published: March 07, 2026

Hb Yongning [β1 (NA1) Val→Leu; HBB:C.4G > C]: A Novel Hemoglobin Variant Causing Significant Interference in Common Glycated Hemoglobin Assays.

Hb Yongning [β1 (NA1) Val→Leu; HBB:C.4G > C]: A Novel Hemoglobin Variant Causing Significant Interference in Common Glycated Hemoglobin Assays.

Journal: Hemoglobin

Published: January 02, 2026

The indispensable role of phenotypic screening in thalassemia diagnosis: a case of deception uncovered by inconsistent results.

The indispensable role of phenotypic screening in thalassemia diagnosis: a case of deception uncovered by inconsistent results.

Journal: Clinical chemistry and laboratory medicine

Published: November 15, 2025

Identification of a novel 10.7 kb deletion (Nanning deletion; -ζ10.7 kb) in a Chinese female.

Identification of a novel 10.7 kb deletion (Nanning deletion; -ζ10.7 kb) in a Chinese female.

Journal: Molecular biology reports

Published: August 04, 2025

The 1357 bp deletion in β-thalassemia: molecular profiling and hematological characterization in a Guangxi cohort.

The 1357 bp deletion in β-thalassemia: molecular profiling and hematological characterization in a Guangxi cohort.

Journal: Molecular biology reports

Published: March 13, 2025

Unveiling the molecular landscape of δ-thalassemia and δ-globin variants in southern China: novel mutations, gene spectrum, and implications for thalassemia diagnosis.

Unveiling the molecular landscape of δ-thalassemia and δ-globin variants in southern China: novel mutations, gene spectrum, and implications for thalassemia diagnosis.

Journal: Frontiers in genetics

Published: February 27, 2025

Genetic screening of α-thalassemia fusion gene using routine flow-through hybridization.

Genetic screening of α-thalassemia fusion gene using routine flow-through hybridization.

Journal: Frontiers in genetics

Published: July 07, 2024

Hb Guigang [α90 (FG2)Lys→Asn; HBA1:c.273G˃T]: a Novel α-Globin Chain Variant.

Hb Guigang [α90 (FG2)Lys→Asn; HBA1:c.273G˃T]: a Novel α-Globin Chain Variant.

Journal: Clinical laboratory

Published: July 05, 2024

Showing 1-12 of 19

Last Updated: 09/26/2026