Microcytosis in patients with haemoglobin C trait: is α‐thalassaemia trait to blame?-Reference-Cited by-同舟云学术

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Microcytosis in patients with haemoglobin C trait: is α‐thalassaemia trait to blame?

Published:2020-09-18 Issue:5 Volume:191 Page:
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br. J. Haematol.

Author:

Forté Stéphanie¹²^ORCID,Eng Barry³,Verhovsek Madeleine⁴^ORCID,Soulières Denis²,Waye John S.³⁵

Affiliation:

1. Division of Medical Oncology and Haematology Department of Medicine University Health Network Toronto Ontario Canada

2. Division of Medical Oncology and Haematology Department of Medicine Centre Hospitalier de l’Université de Montréal (CHUM) Montréal Québec Canada

3. Hamilton Regional Laboratory Medicine Program Hamilton Health Sciences Hamilton Ontario Canada

4. Division of Haematology and Thromboembolism Department of Medicine McMaster University Hamilton Ontario Canada

5. Department of Pathology and Molecular Medicine McMaster University Hamilton Ontario Canada

Publisher

Wiley

Subject

Hematology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjh.17095

Reference7 articles.

1. The distribution of haemoglobin C and its prevalence in newborns in Africa

2. Haemoglobinopathy Diagnosis

3. α-Thalassemia 2, 3.7 kb deletion and hemoglobin AC heterozygosity in pregnancy: a molecular and hematological analysis

4. Laboratory parameters provided by Advia 2120 analyser identify structural haemoglobinopathy carriers and discriminate between Hb S trait and Hb C trait

5. Trimodality in Tie Percentages of β Chain Variants in Heterozy-Gotes: The Effect of the Number of Aczive HBαStructural Loci

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