Chi-chiu J. So

Sar, China

Last Updated: 09/26/2026

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Found 23 publications

NGS4THAL, a One-Stop Molecular Diagnosis and Carrier Screening Tool for Thalassemia and Other Hemoglobinopathies by Next-Generation Sequencing.

NGS4THAL, a One-Stop Molecular Diagnosis and Carrier Screening Tool for Thalassemia and Other Hemoglobinopathies by Next-Generation Sequencing.

Journal: The Journal of molecular diagnostics : JMD
Published: June 29, 2021

Congenital Hemolytic Anemia Because of Glucose Phosphate Isomerase Deficiency: Identification of 2 Novel Missense Mutations in the GPI Gene.

Congenital Hemolytic Anemia Because of Glucose Phosphate Isomerase Deficiency: Identification of 2 Novel Missense Mutations in the GPI Gene.

Journal: Journal of pediatric hematology/oncology
Published: August 16, 2019

A molecular study on the role of alpha-hemoglobin-stabilizing protein in hemoglobin H disease.

A molecular study on the role of alpha-hemoglobin-stabilizing protein in hemoglobin H disease.

Journal: Annals of hematology
Published: October 20, 2016

Homoharringtonine (omacetaxine mepesuccinate) as an adjunct for FLT3-ITD acute myeloid leukemia.

Homoharringtonine (omacetaxine mepesuccinate) as an adjunct for FLT3-ITD acute myeloid leukemia.

Journal: Science translational medicine
Published: February 01, 2016

Dysregulation of the intrinsic apoptotic pathway mediates megakaryocytic hyperplasia in myeloproliferative neoplasms.

Dysregulation of the intrinsic apoptotic pathway mediates megakaryocytic hyperplasia in myeloproliferative neoplasms.

Journal: Journal of clinical pathology
Published: January 14, 2016

Curative Stem Cell Transplantation for Severe Hb H Disease Manifesting From Early Infancy: Phenotypic and Genotypic Analyses.

Curative Stem Cell Transplantation for Severe Hb H Disease Manifesting From Early Infancy: Phenotypic and Genotypic Analyses.

Journal: Hemoglobin
Published: November 18, 2015

Subtle skin involvement in nodal γδ peripheral T-cell lymphoma.

Subtle skin involvement in nodal γδ peripheral T-cell lymphoma.

Journal: The Journal of dermatology
Published: January 24, 2015

Genetic basis of persistent red blood cell microcytosis in the Chinese unexplained by phenotypical testing.

Genetic basis of persistent red blood cell microcytosis in the Chinese unexplained by phenotypical testing.

Journal: Journal of clinical pathology
Published: October 30, 2014

Alpha thalassemia trait masquerading as hemoglobin H disease due to co-existing primary myelofibrosis.

Alpha thalassemia trait masquerading as hemoglobin H disease due to co-existing primary myelofibrosis.

Journal: Annals of hematology
Published: September 27, 2014

Beta thalassaemia intermedia due to silent alpha globin gene quadruplication in an infant.

Beta thalassaemia intermedia due to silent alpha globin gene quadruplication in an infant.

Journal: Pathology
Published: August 28, 2014

A comparison of high resolution melting, allele-specific priming and Sanger sequencing for the detection of BRAFV600E mutation in hairy cell leukaemia from different haematological specimens.

A comparison of high resolution melting, allele-specific priming and Sanger sequencing for the detection of BRAFV600E mutation in hairy cell leukaemia from different haematological specimens.

Journal: Pathology
Published: August 28, 2014

Novel point mutation of the α2-globin gene (HBA2) and a rare 2.4 kb deletion of the α1-globin gene (HBA1), identified in two chinese patients with Hb H disease.

Novel point mutation of the α2-globin gene (HBA2) and a rare 2.4 kb deletion of the α1-globin gene (HBA1), identified in two chinese patients with Hb H disease.

Journal: Hemoglobin
Published: May 16, 2014
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Last Updated: 09/26/2026