The Development of Haemoglobin A2in Normal Negro Infants and in Sickle Cell Disease-Reference-Cited by-同舟云学术

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The Development of Haemoglobin A2in Normal Negro Infants and in Sickle Cell Disease

Published:1978-06 Issue:2 Volume:39 Page:259-265
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Serjeant B. E.,Mason K. P.,Serjeant G. R.

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1978.tb01096.x/fullpdf

Reference11 articles.

1. Comparison of Haematological Features of the β0and β+Thalassaemia Traits in Jamaican Negroes

2. The Clinical Features of Sickle-Cell/β Thalassaemia in Jamaica

Cited by 17 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. The beta thalassaemia trait in Jamaica;Journal of Community Genetics;2023-06-30

2. Phenotypic variation in sickle cell disease: the role of beta globin haplotype, alpha thalassemia, and fetal hemoglobin in HbSS;Expert Review of Hematology;2022-02-01

3. Sickle cell haemoglobin and its interactions with other variant haemoglobins and with thalassaemias;Haemoglobinopathy Diagnosis;2020-02-28

4. α, β, δ and γ thalassaemias and related conditions;Haemoglobinopathy Diagnosis;2020-02-28

5. Haemoglobin and the genetics of haemoglobin synthesis;Haemoglobinopathy Diagnosis;2020-02-28

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