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Article

Alpha-thalassaemia.

Bailliere's clinical haematology - 1 Mar 1998

Bernini L F, Harteveld C L

Abstract excerpt

alpha-Thalassaemias are genetic defects extremely frequent in some populations and are characterized by the decrease or complete suppression of alpha-globin polypeptide chains. The gene cluster, which codes for and controls the production of these polypeptides, maps near the telomere of the short arm of chromosome 16, within a G + C rich and early-replicating DNA region. The genes expressed during the embryonic...

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PMID: 10872473
DOI: 10.1016/s0950-3536(98)80070-x

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

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