Haemoglobin Hope in a northern Thai family: first identification of homozygous haemoglobin Hope associated with haemoglobin H disease
Author:
Publisher
Wiley
Subject
Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.2007.00907.x/fullpdf
Reference14 articles.
1. Heterozygous Hb Hope [β136(H14)Gly→Asp] in Association with Heterozygous β0-Thalassemia with Apparent Homozygous Expression, in a Spanish Patient
2. Hb Hope [β136(H14)Gly→Asp (GGT→GAT)]: Interactions with Hb S [β6(A3)Glu→Val (GAG→GTG)], Other Variant Hemoglobins and Thalassemia
3. Molecular and Hematological Characterization of Hemoglobin Hope/Hemoglobin E and Hemoglobin Hope/a-Thalassemia 2 in Thai Patients
4. HbHope/HbS and HbS/?-thal double compound heterozygosity in a Mauritanian family: clinical and biochemical studies
5. HB Hope [B136(H14)GLY→ASP] and HB E [D26 (B8) GLU→LYS] : Compound Heterozygosity in a Thai Mien Family
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1. Molecular epidemiology, pathogenicity, and structural analysis of haemoglobin variants in the Yunnan province population of Southwestern China;Scientific Reports;2019-06-04
2. Development of hemoglobin typing control materials for laboratory investigation of thalassemia and hemoglobinopathies;Clinical Chemistry and Laboratory Medicine (CCLM);2016-01-01
3. Detection of Co-inheritance of Hb Hope and Hb Constant Spring in Three Thai Samples by Capillary Electrophoresis;Indian Journal of Hematology and Blood Transfusion;2015-09-14
4. Detection of Abnormal Hemoglobin Variants by HPLC Method: Common Problems with Suggested Solutions;International Scholarly Research Notices;2014-10-12
5. Variable Genotype-Phenotype Correlations in Patients With a Rare Nondeletional α-thalassemia; Hb Pak Num Po (HBA1;Journal of Pediatric Hematology/Oncology;2014-04
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