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Article

Genotype/Phenotype Correlation of β-Thalassemia in Syrian Patients: A Cross-Sectional Study.

Hemoglobin - 1 Jan 2020

Shoujaa Ahmad, Moasses Faten, Mukhalalaty Yasser, Murad Hossam, Al-Quobaili Faizeh

Abstract excerpt

β-Thalassemia (β-thal) is an inherited blood disorder caused by reduced or absent synthesis of β-globin chains leading to imbalance of globin chain synthesis. β0-Thalassemia (β0-thal), refers to the complete absence of β-globin chain production on the affected allele. β+-Thalassemia (β+-thal) refers to alleles with some residual production of β-globin chain. We studied the correlation of genotype/phenotype of...

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Identifiers

PMID: 31903828
DOI: 10.1080/03630269.2019.1709207

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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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