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Article

HbS/beta(del)-thalassemia associated with high levels of hemoglobins A2 and F in a Turkish family.

American journal of hematology - 1 Sept 1998

Tadmouri G O, Yüksel L, Başak A N

Abstract excerpt

Beta-thalassemia and sickle cell disease (SCD) are common disorders in Turkey. Compound heterozygosity for these two disorders (betaS/beta-thalassemia) is encountered frequently. In this report we present hematological and molecular data of two Turkish siblings with betaS/beta(del)-thalassemia caused by a 290 base pair (bp) deletion and associated with increased levels of hemoglobin A2 (HbA2) and hemoglobin F...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 9723583
DOI: 10.1002/(sici)1096-8652(199809)59:1<83::aid-ajh16>3.0.co;2-2

Genes

SCD

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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