Shiqiang Luo

Nanning, China

Last Updated: 09/26/2026

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Found 15 publications

Distribution characteristics and clinical phenotype analyses of hemoglobin variants in the Z region of Central Guangxi, Southern China.

Distribution characteristics and clinical phenotype analyses of hemoglobin variants in the Z region of Central Guangxi, Southern China.

Journal: Hematology (Amsterdam, Netherlands)

Published: March 30, 2023

Detection of four rare thalassemia variants using Single-molecule realtime sequencing.

Detection of four rare thalassemia variants using Single-molecule realtime sequencing.

Journal: Frontiers in genetics

Published: June 21, 2022

Correction to: The value of single-molecule real-time technology in the diagnosis of rare thalassemia variants and analysis of phenotype-genotype correlation.

Correction to: The value of single-molecule real-time technology in the diagnosis of rare thalassemia variants and analysis of phenotype-genotype correlation.

Journal: Journal of human genetics

Published: November 24, 2021

Identification and Functional Characterization of a Novel Nonsense Variant in ARR3 in a Southern Chinese Family With High Myopia.

Identification and Functional Characterization of a Novel Nonsense Variant in ARR3 in a Southern Chinese Family With High Myopia.

Journal: Frontiers in genetics

Published: August 27, 2021

The value of single-molecule real-time technology in the diagnosis of rare thalassemia variants and analysis of phenotype-genotype correlation.

The value of single-molecule real-time technology in the diagnosis of rare thalassemia variants and analysis of phenotype-genotype correlation.

Journal: Journal of human genetics

Published: July 29, 2021

Concurrent Newborn Hearing and Genetic Screening in a Multi-Ethnic Population in South China.

Concurrent Newborn Hearing and Genetic Screening in a Multi-Ethnic Population in South China.

Journal: Frontiers in pediatrics

Published: July 21, 2021

Application of Copy Number Variation Sequencing in Genetic Analysis of Miscarriages in Early and Middle Pregnancy.

Application of Copy Number Variation Sequencing in Genetic Analysis of Miscarriages in Early and Middle Pregnancy.

Journal: Cytogenetic and genome research

Published: August 15, 2020

Analysis of Hb levels and degree of anemia in relation to genotype in 615 patients with hemoglobin H disease.

Analysis of Hb levels and degree of anemia in relation to genotype in 615 patients with hemoglobin H disease.

Journal: Expert review of hematology

Published: July 31, 2020

Analysis of rare thalassemia caused by HS-40 regulatory site deletion.

Analysis of rare thalassemia caused by HS-40 regulatory site deletion.

Journal: Hematology (Amsterdam, Netherlands)

Published: July 29, 2020

Analysis of beta-globin gene variants in Liuzhou area of Guangxi

Analysis of beta-globin gene variants in Liuzhou area of Guangxi

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics

Published: March 29, 2020

Diagnosis and Prenatal Diagnosis in a Chinese Family Carrying the Rare α-Thalassemia Gene HBA2: c.1A>G Mutation.

Diagnosis and Prenatal Diagnosis in a Chinese Family Carrying the Rare α-Thalassemia Gene HBA2: c.1A>G Mutation.

Journal: Hemoglobin

Published: January 15, 2020

Characterization of two novel Alu element-mediated α-globin gene cluster deletions causing α0-thalassemia by targeted next-generation sequencing.

Characterization of two novel Alu element-mediated α-globin gene cluster deletions causing α0-thalassemia by targeted next-generation sequencing.

Journal: Molecular genetics and genomics : MGG

Published: August 19, 2019

Showing 1-12 of 15

Last Updated: 09/26/2026