Characterization of a new α° thalassaemia defect in the South African population-Reference-Cited by-同舟云学术

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Characterization of a new α° thalassaemia defect in the South African population

Published:1987-08 Issue:4 Volume:66 Page:539-542
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:Br J Haematol

Author:

Vandenplas S.,Higgs D. R.,Nicholls R. D.,Bester A. J.,Mathew C. G. P.

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1987.tb01341.x/fullpdf

Reference26 articles.

1. The haemoglobin H disease mental retardation syndrome: molecular studies on the South African case

2. The Molecular Genetics of Human Hemoglobin

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1. Revisiting and updating molecular epidemiology of α-thalassemia mutations in Thailand using MLPA and new multiplex gap-PCR for nine α-thalassemia deletion;Scientific Reports;2023-06-17

2. Molecular Heterogeneity of Hb H Disease in India;Thalassemia Reports;2022-07-06

3. Breakpoint characterization of a rare alpha 0 ‐thalassemia deletion using targeted locus amplification on genomic DNA;International Journal of Laboratory Hematology;2021-07-12

4. Molecular spectrum of Hb H disease and characterization of rare deletional α-thalassemia found in Thailand;Scandinavian Journal of Clinical and Laboratory Investigation;2020-07-29

5. Fine-tiling array CGH to improve diagnostics for α- and β-thalassemia rearrangements;Human Mutation;2011-10-31

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