Thalassemia intermedia in HbH-CS disease with compound heterozygosity for .BETA.-thalassemia: Challenges in hemoglobin analysis and clinical diagnosis-Reference-Cited by-同舟云学术

Thalassemia intermedia in HbH-CS disease with compound heterozygosity for .BETA.-thalassemia: Challenges in hemoglobin analysis and clinical diagnosis

Published:2009 Issue:1 Volume:84 Page:67-71
ISSN:1341-7568
Container-title:Genes & Genetic Systems
language:en
Short-container-title:Genes Genet. Syst.

Author:

Tan Jin Ai Mary Anne¹,Kok Juan Loong²,Tan Kim Lian¹,Wee Yong Chui¹,George Elizabeth³

Affiliation:

1. Department of Molecular Medicine, Faculty of Medicine, University of Malaya

2. Pediatrics Department, Hospital Kuching

3. Hematology Unit, Department of Pathology, Faculty of Medicine and Health Sciences University Putra Malaysia

Publisher

Genetics Society of Japan

Subject

Genetics,Molecular Biology,General Medicine

Link

http://www.jstage.jst.go.jp/article/ggs/84/1/84_1_67/_pdf

Reference23 articles.

1. Detection of common deletional α-thalassemia-2 determinants by PCR

2. Different Forms of Hb H Disease in the Chinese

3. Hemoglobin H disease: not necessarily a benign disorder

4. Haemoglobin Constant Spring—A Chain Termination Mutant ?

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