Hb nijkerk: A new mutation at codons 138/139 of the β-giobin gene inducing severe hemolytic anemia in a dutch girl-Reference-Cited by-同舟云学术

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Hb nijkerk: A new mutation at codons 138/139 of the β-giobin gene inducing severe hemolytic anemia in a dutch girl

Published:1999-01 Issue:2 Volume:23 Page:135-144
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

van den Berg H. M.,Bruin M. C. A.,Batelaan D.,Delft P. van,Zwieten R. van,Roos D.,Harteveld C. L.,Bernini L. F.,Giordano P. C.

Publisher

Informa UK Limited

Subject

Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology

Link

http://www.tandfonline.com/doi/pdf/10.3109/03630269908996158

Reference18 articles.

1. Rapid estimation of hemoglobin A2 by DEAE chromatography

2. Estimation of Small Percentages of Fœtal Hæmoglobin

Cited by 8 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. Strategies for basic laboratory diagnostics of the hemoglobinopathies in multi-ethnic societies: interpretation of results and pitfalls;International Journal of Laboratory Hematology;2012-12-07

2. Newborn Screening for Hemoglobinopathies Using Capillary Electrophoresis;Methods in Molecular Biology;2012-07-26

3. Dominantly Inherited β-Thalassemia;Hemoglobin;2007-01

4. Hb Jambol: A New Hyperunstable Hemoglobin Causing Severe Hemolytic Anemia;Acta Haematologica;2006-11-08

5. A deletion of 11 bp (CD 131–134) in exon 3 of the β-globin gene produces the phenotype of inclusion body β-thalassemia;Annals of Hematology;2005-06-24

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