Rare form of autosomal dominant thalassemia-Hemoglobin Hakkari-Reference-Cited by-同舟云学术

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Rare form of autosomal dominant thalassemia-Hemoglobin Hakkari

Published:2014-05-02 Issue:11 Volume:61 Page:2118-2120
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatr Blood Cancer

Author:

Nair Sushmita¹,Eldjerou Lamis K¹,Harris Neil S.²,Dunbar Levette N.¹^ORCID

Affiliation:

1. Division of Pediatric Hematology and Oncology; Department of Pediatrics; University of Florida; Gainesville Florida

2. Division of Pathology; University of Florida; Gainesville Florida

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/pbc.25082/fullpdf

Reference20 articles.

1. The beta-thalssemias;Olivieri;N Engl J Med,1999

2. Pathophysiology of thalssemia;Schier;Curr Opin Hematol,2002

3. Structural hemoglobin variants that produce the phenotype of thalassemia;Adams;Semin Hematol,1990

4. Thalassemic hemoglobinopathies;Steinberg;Am J Pathol,1983

5. The unstable hemoglobins;Williamson;Blood Rev,1993

Cited by 3 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. Rare unstable hemoglobin Hakkari in Russia: a case report and literature review;Pediatric Hematology/Oncology and Immunopathology;2022-10-15

2. De novo HBB frameshift mutation in a patient with dominant β‐thalassemia major;International Journal of Laboratory Hematology;2021-07-29

3. Clinical Genotyping by Next Generation Sequencing Reveals a Novel, De Novo β-Globin Gene Mutation Causing Hemolytic Anemia in a Chinese Individual;Hemoglobin;2018-05-04

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