Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Alpha-thalassaemia and beta-thalassaemia traits: biological difference based on red cell indices and zinc protoporphyrin.

Clinical and laboratory haematology - 1 Jan 1990

Han P, Fung K P, Teo C P, Tam L P

Abstract excerpt

alpha-thalassaemia and beta-thalassaemia traits are two commonly encountered haemoglobinopathies in South East Asia. Both present with hypochromia and microcytosis. The use of modern electronic or optical cell counters which measure accurately the red cell parameters has allowed for an initial quick screening for the presence of thalassaemia. Seven red cell parameters were measured by the Technicon H1 cell...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adolescent
Share to Aged
Share to Aged, 80 and over

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

Share to Biomarkers

Share to Diagnosis, Differential

Share to Discriminant Analysis

Share to Phenotype

Share to Thalassemia

Source

Identifiers

PMID: 2208947

Provenance

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.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 8 closest

Alpha-thalassaemia and beta-thalassaemia traits: biological difference based on red cell indices and zinc protoporphyrin.PMID 2208947Read ↗

Alpha-thalassaemia.Semantic proximity Read ↗

RBC-Y/MCV as a discriminant function for differentiating carriers of thalassaemia and HbE from iron deficiency.Semantic proximity Read ↗

The G6PD flow-cytometric assay is a reliable tool for diagnosis of G6PD deficiency in women and anaemic subjects.Semantic proximity Read ↗

Diagnosis of Hemoglobinopathies and thalassemias using both Haemoglobin capillary zone electrophoresis and High performance liquid chromatography - An experience from a tertiary care hospital in Northern IndiaSemantic proximity Read ↗

Cut-Off Values of Hematologic Parameters to Predict the Number of Alpha Genes Deleted in Subjects with Deletional Alpha ThalassemiaSemantic proximity Read ↗

Erythrocyte volume and haemoglobin concentration in haemoglobin H disease: discrimination between the two genotypes.Semantic proximity Read ↗

Diagnostic applications of newborn screening for α-thalassaemias, haemoglobins E and H disorders using isoelectric focusing on dry blood spots.Semantic proximity Read ↗

The contribution of alpha+-thalassaemia to anaemia in a Nigerian population exposed to intense malaria transmission.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.