MOLECULAR CHARACTERIZATION OF Hb D-IBADAN [β87(F3)Thr→Lys] IN COMBINATION WITH Hb S [β(A3)Glu→Val] AND WITHβ+-THALASSEMIA: REPORT OF TWO CASES-Reference-Cited by-同舟云学术

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MOLECULAR CHARACTERIZATION OF Hb D-IBADAN [β87(F3)Thr→Lys] IN COMBINATION WITH Hb S [β(A3)Glu→Val] AND WITHβ+-THALASSEMIA: REPORT OF TWO CASES

Published:2002-01 Issue:2 Volume:26 Page:129-134
ISSN:0363-0269
Container-title:Hemoglobin
language:en
Short-container-title:Hemoglobin

Author:

Redding-Lallinger Rupa,Tankut Gaye,Holley Leslie,Wright Frances,Kutlar Abdullah,Kutlar Ferdane

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.1081/HEM-120005450

Reference9 articles.

1. A New Haemoglobin, D Ibadan (β-87 Threonine → Lysine), Producing No Sickle-Cell Haemoglobin D Disease with Haemoglobin S

2. Hemoglobin D Ibadan Trait in Combination with δβ Thalassemia

Cited by 10 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. Compound Heterozygosity for Hb D-Ibadan (HBB: c.263C>A) and Hb C (HBB: c.19G>A);Hemoglobin;2018-07-04

2. Hemoglobin F Only Syndrome at Birth;Journal of Pediatric Hematology/Oncology;2016-01

3. Two New Hemoglobin Variants: Hb Tallahassee [α3(A1)Ser→Tyr;HBA2: c.11C>A] and Hb Madison-NC [β119(GH2)Gly→Ser;HBB: c.358G>A];Hemoglobin;2014-01-29

4. Hb Fulton-Georgia [α20(B1)His→Pro;HBA1: c.62A>C]: A New α-Globin Variant Coinherited with α-Thalassemia-2 (3.7 kb deletion) and Hb SC Disease;Hemoglobin;2013-07-03

5. Thalassemia-like Phenotype in a Novel Complex Hemoglobinopathy With α, β, δ Globin Chain Abnormalities;Journal of Pediatric Hematology/Oncology;2011-12

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