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Article

The expanding spectrum of thalassemia intermedia.

Hematology (Amsterdam, Netherlands) - 1 Dec 2009

Panigrahi Inusha, Marwaha Ram K, Kulkarni Ketan

Abstract excerpt

The hemoglobin disorders serve as a model for study of the genetic heterogeneity underlying the phenotype of genetic disorders. 'Thalassemia intermedia' is a clinical phenotype which displays marked genotypic variability in different populations or ethnic groups. Two common underlying mechanisms include co-inheritance of alpha globin gene deletions in homozygous thalassemia intermedia and presence of XmnI...

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PMID: 19941736
DOI: 10.1179/102453309X12473408860307

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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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