Short Communication:HB Taybe: Description of Genetics and Laboratory Findings in an Israeli Arab Family
Author:
Publisher
Informa UK Limited
Subject
Biochemistry, medical,Clinical Biochemistry,Genetics(clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630269809092141
Reference7 articles.
1. Compound heterozygosity for two α-globin gene defects, Hb taybe (α1; 38 or 39 minus thr) and a poly a mutation (α2; AATAAA → AATAAG), results in a severe hemolytic anemia
2. Unstable alpha-chain hemoglobin variants with factitious beta-thalassemia biosynthetic ratio: Hb questembert (α131[H14] Ser→Pro) and Hb Caen (α132[H15] Val→Gly)
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1. Hb TAYBE: clinical and morphological findings IN 43 patients;European Journal of Haematology;2015-12-15
2. Thrombosis in Hb Taybe [codons 38/39 (–ACC) (α1)];Hemoglobin;2012-08
3. First Detection of Hb Taybe [α38(C3) or α39(C4) Thr→0 (α1)] in An Italian Child;Hemoglobin;2012-03-19
4. First Observation of Hb Taybe [Codons 38/39 (−Acc) Thr→0 (α1)] In Greece: Clinical and Hematological Findings in Patients With Co-Inherited α+-Thalassemia Mutations;Hemoglobin;2008-01
5. Hydrops fetalis associated with homozygosity for hemoglobin Taybe (? 38/39 THR deletion) in newborn triplets;American Journal of Hematology;2004
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