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

Application of an expanded multiplex genotyping assay for the simultaneous detection of Hemoglobin Constant Spring and common deletional alpha-thalassemia mutations.

International journal of laboratory hematology - 1 Aug 2010

Kidd J L, Azimi M, Lubin B, Vichinsky E, Hoppe C

Abstract excerpt

Hemoglobin Constant Spring (HbCS) is the most common nondeletional alpha-thalassemia variant causing HbH disease, making its detection crucial in populations at risk. Universal newborn screening for HbH is carried out in California. Identification of alpha-thalassemia genotypes responsible for Hb...

Read the complete abstract on PubMed

Topics

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

Share to alpha-Thalassemia
Share to California
Share to Follow-Up Studies

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genotype

Share to Hemoglobins, Abnormal

Share to Infant, Newborn

Share to Polymerase Chain Reaction

Share to Sequence Deletion

Source

Identifiers

PMID: 19919622
DOI: 10.1111/j.1751-553X.2009.01197.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19919622-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Application of an expanded multiplex genotyping assay for the simultaneous detection of Hemoglobin Constant Spring and common deletional alpha-thalassemia mutations.PMID 19919622Read ↗

Newborn screening for hemoglobinopathies in CaliforniaSemantic proximity Read ↗

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

Universal newborn screening for Hb H disease in California.Semantic proximity Read ↗

Application of flow cytometry-based genotyping for rapid detection of hemoglobin variants.Semantic proximity Read ↗

Identification of Hb Constant Spring (HBA2: c.427T > C) by an Automated High Performance Liquid Chromatography Method.Semantic proximity Read ↗

Laboratory investigations of Hb Constant Spring.Semantic proximity Read ↗

Molecular assay of -alpha(3.7) and -alpha(4.2) deletions causing alpha-thalassemia by denaturing high-performance liquid chromatography.Semantic proximity Read ↗

[Analysis of the phenotype-genotype relationship of Hb Constant Spring].Semantic proximity Read ↗

Hematological Characteristics of Hb Constant Spring (HBA2: c.427T>C) Carriers in Mainland China.Semantic proximity Read ↗

Detection of Hb Constant Spring (HBA2: c.427T>C) Heterozygotes in Combination with β-Thalassemia or Hb E Trait by Capillary Electrophoresis.Semantic proximity Read ↗

Heterogeneity of hemoglobin H disease in childhood.Semantic proximity Read ↗

Direct PCR assays without DNA extraction for rapid detection of hemoglobin Constant Spring and Pakse' genes: application for carrier screening and prenatal diagnosis.Semantic proximity Read ↗

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