?-thalassemia in association with a new ?-chain hemoglobin variant [?116(g18)Arg?Leu]: Implications for carrier screening and prenatal diagnosis-Reference-Cited by-同舟云学术

?-thalassemia in association with a new ?-chain hemoglobin variant [?116(g18)Arg?Leu]: Implications for carrier screening and prenatal diagnosis

Published:2003-10-24 Issue:3 Volume:74 Page:179-181
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am. J. Hematol.

Author:

Waye John S.,Patterson Margaret,Walker Lynda,Eng Barry,Nakamura Lisa M.,Lafferty John D.,Yong Sui-Li,Wu John K.,Chui David H.K.

Publisher

Wiley

Subject

Hematology

Reference14 articles.

1. Clinical and laboratory features of the ?-thalassemia syndromes. In: editors. Disorders of hemoglobin: genetics, pathophysiology, and clinical management. Cambridge, UK: Cambridge University Press; 2001.

2. The ?? and related thalassaemias. In: editors. The thalassaemia syndromes, 4th ed. London: Blackwell Science; 2001.

3. Identification of HB Lepore-Mashington-Boston in Association with HB E [βB26(B8)GLU→LYS] in a Thai Female

4. Hb E/Hb LeporeHollandia in a family from Bangladesh

5. Complex interactions of δβ hybrid haemoglobin (Hb Lepore-Hollandia) Hb E (β26 G→A ) and α+ thalassaemia in a Thai family

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. Borderline HbA2 levels: Dilemma in diagnosis of beta-thalassemia carriers;Mutation Research/Reviews in Mutation Research;2021-07

2. Diverse hematological phenotypes of β-thalassemia carriers;Annals of the New York Academy of Sciences;2016-03

3. Normal Hb A2β-Thalassemia Trait: Frameshift Mutation (HBB: c.187_251dup) inCiswith the Hb A2’δ-Globin Gene Missense Mutation (HBD: c.49G>C);Hemoglobin;2013-02-11

4. The Prevention of Thalassemia;Cold Spring Harbor Perspectives in Medicine;2013-02-01

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