Delineation of the molecular basis of borderline hemoglobin A2 in Chinese individuals-Reference-Cited by-同舟云学术

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Delineation of the molecular basis of borderline hemoglobin A2 in Chinese individuals

Published:2014-12 Issue:4 Volume:53 Page:261-264
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Lou Ji-Wu,Li Dong-Zhi,Zhang Yu,He Yi,Sun Man-Na,Ye Wan-Ling,Liu Yan-Hui

Funder

Dongguan Science and Technology Bureau

Publisher

Elsevier BV

Subject

Cell Biology,Hematology,Molecular Biology,Molecular Medicine

Reference26 articles.

1. Global epidemiology of haemoglobin disorders and derived service indicators;Modell;Bull. World Health Organ.,2008

2. The role of haemoglobin A(2) testing in the diagnosis of thalassaemias and related haemoglobinopathies;Mosca;J. Clin. Pathol.,2009

3. Significance of borderline hemoglobin A2 values in an Italian population with a high prevalence of beta-thalassemia;Giambona;Haematologica,2008

4. New analytical tools and epidemiological data for the identification of HbA2 borderline subjects in the screening for beta-thalassemia;Mosca;Bioelectrochemistry,2008

5. Genotype of subjects with borderline hemoglobin A2 levels: implication for beta-thalassemia carrier screening;Galanello;Am. J. Hematol.,1994

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2. Unresolved laboratory issues of the heterozygous state of β-thalassemia: a literature review;Haematologica;2023-06-01

3. A stepwise haematological screening and whole‐exome sequencing reveal multiple mutations from SUPT5H causing an elevation of Hb A ₂ from a cohort of 47336 individuals;International Journal of Laboratory Hematology;2022-08-24

4. Severe neonatal haemolytic anaemia caused by compound heterozygous KLF1 mutations: report of four families and literature review;British Journal of Haematology;2021-07-05

5. Borderline HbA2 levels: Dilemma in diagnosis of beta-thalassemia carriers;Mutation Research/Reviews in Mutation Research;2021-07

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