Man-yu Wu

Guangzhou, China

Last Updated: 09/26/2026

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Found 9 publications

A novel selective deletion of the major α-globin regulatory element (MCS-R2) causing α-thalassaemia.

A novel selective deletion of the major α-globin regulatory element (MCS-R2) causing α-thalassaemia.

Journal: British journal of haematology

Published: February 27, 2016

The Codon 35 (A > G) (HBB: c.107A > G) at the α-β Chain Interface of the β-Globin Gene: A Silent Mutation?

The Codon 35 (A > G) (HBB: c.107A > G) at the α-β Chain Interface of the β-Globin Gene: A Silent Mutation?

Journal: Hemoglobin

Published: January 13, 2016

First Detection of the -27 (A > G) (HBB: c.-77A > G) Mutation of the β-Globin Gene in a Chinese Family.

First Detection of the -27 (A > G) (HBB: c.-77A > G) Mutation of the β-Globin Gene in a Chinese Family.

Journal: Hemoglobin

Published: November 12, 2015

Evidence of Selection for the α-Globin Gene Deletions and Triplications in a Southern Chinese Population.

Evidence of Selection for the α-Globin Gene Deletions and Triplications in a Southern Chinese Population.

Journal: Hemoglobin

Published: August 21, 2015

Frequencies of HKαα and anti-HKαα Alleles in Chinese Carriers of Silent Deletional α-Thalassemia.

Frequencies of HKαα and anti-HKαα Alleles in Chinese Carriers of Silent Deletional α-Thalassemia.

Journal: Hemoglobin

Published: August 20, 2015

Thalassemia Intermedia Caused by 16p13.3 Sectional Duplication in a β-Thalassemia Heterozygous Child.

Thalassemia Intermedia Caused by 16p13.3 Sectional Duplication in a β-Thalassemia Heterozygous Child.

Journal: Pediatric hematology and oncology

Published: June 19, 2015

Compound Heterozygosity for HKαα and an in Cis Deletion of Double α Genes Presents as α-Thalassemia Trait.

Compound Heterozygosity for HKαα and an in Cis Deletion of Double α Genes Presents as α-Thalassemia Trait.

Journal: Hemoglobin

Published: May 29, 2015

The Frequency of α-Globin Gene Triplication in a Southern Chinese Population.

The Frequency of α-Globin Gene Triplication in a Southern Chinese Population.

Journal: Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion

Published: February 11, 2015

A Novel Mutation of Ribosomal Protein S19 Gene in a Chinese Child with Diamond-Blackfan Anemia.

A Novel Mutation of Ribosomal Protein S19 Gene in a Chinese Child with Diamond-Blackfan Anemia.

Journal: Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion

Published: January 17, 2015

Showing 1-9 of 9

Last Updated: 09/26/2026