Phenotypic expression of Hb F in common high Hb F determinants in Thailand: roles ofα-thalassemia, 5′ δ-globin BCL11A binding region and 3′ β-globin enhancer-Reference-Cited by-同舟云学术

Phenotypic expression of Hb F in common high Hb F determinants in Thailand: roles ofα-thalassemia, 5′ δ-globin BCL11A binding region and 3′ β-globin enhancer

Published:2013-10-24 Issue:1 Volume:92 Page:73-79
ISSN:0902-4441
Container-title:European Journal of Haematology
language:en
Short-container-title:Eur J Haematol

Author:

Prakobkaew Nattaphol¹²,Fucharoen Supan²,Fuchareon Goonnapa²,Siriratmanawong Nirut³

Affiliation:

1. The Graduate School; Khon Kaen University; Khon Kaen Thailand

2. Centre for Research and Development of Medical Diagnostic Laboratories; Faculty of Associated Medical Sciences; Khon Kaen University; Khon Kaen Thailand

3. Regional Health Promotion Center, region 8; Nakhon Sawan Thailand

Publisher

Wiley

Subject

Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ejh.12201/fullpdf

Reference21 articles.

1. Hemoglobinopathies in Southeast Asia;Fucharoen;Hemoglobin,1987

2. Molecular characterization of (δβ)o/βo- thalassemia and (δβ)o-thalassemia/Hb E in Thai patients;Fucharoen;Eur J Haematol,2001

3. Molecular and hematological characterization of HPFH-6/Indian deletion-inversion Gγ(Aγδβ)0-Thalassemia and Gγ(Aγδβ)0-Thalassemia/HbE in Thai Patients;Fucharoen;Am J Hematol,2002

4. Transcriptional silencing of fetal hemoglobin by BCL11A;Sankaran;Ann N Y Acad Sci,2010

5. Rapid detection of deletions causing delta beta thalassemia and hereditary persistence of fetal hemoglobin by enzymatic amplification;Craig;Blood,1994

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