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

Topics Community

Article

Hematological characteristics and effective screening for compound heterozygosity for Hb constant spring and deletional α+ -thalassemia.

American journal of hematology - 1 Jul 2011

Uaprasert Noppacharn, Rojnuckarin Ponlapat, Settapiboon Rung, Amornsiriwat Supaporn, Sutcharitchan Pranee

Abstract excerpt

No abstract is available from the source.

Topics

Alleles
Area Under Curve
Female
Genetic Carrier Screening
Hemoglobins, Abnormal
Heterozygote
Humans
Male
Sequence Deletion
Thailand
alpha-Thalassemia

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 21509802
DOI: 10.1002/ajh.22033

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Hematological characteristics and effective screening for compound heterozygosity for Hb constant spring and deletional α+ -thalassemia.PMID 21509802Read ↗

[The haematological phenotype and genotype analysis on 14 co-inheritance of hemoglobin Constant Spring and β-thalassemia].Semantic proximity Read ↗

Molecular characteristics of α+-thalassemia (3.7 kb deletion) in Southeast Asia: Molecular subtypes, haplotypic heterogeneity, multiple founder effects and laboratory diagnosticsSemantic proximity Read ↗

A simple screening test for abnormal hemoglobins and their traits.Semantic proximity Read ↗

Mild Hb Constant Spring-Hb H disease with beta zero-thalassemia trait.Semantic proximity Read ↗

Detection of the heterozygote of hemoglobin Constant Spring by α-thalassemia immunochromatographic strip test.Semantic proximity Read ↗

EMQN Best Practice Guidelines for molecular and haematology methods for carrier identification and prenatal diagnosis of the haemoglobinopathies.Semantic proximity Read ↗

Genotype-phenotype correlation in patients with deletional and nondeletional mutations of Hb H disease in Southwest of Iran.Semantic proximity Read ↗

Hemoglobinopathies.Semantic proximity Read ↗

Detection and prevention of important alpha-thalassemia variants.Semantic proximity Read ↗

Molecular diagnosis of inherited disorders: lessons from hemoglobinopathies.Semantic proximity Read ↗

Hemoglobin variants: biochemical properties and clinical correlates.Semantic proximity Read ↗

Development of DNA analysis for human diseases. Sickle cell anemia and thalassemia as a paradigm.Semantic proximity Read ↗

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