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

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

JAMA - 18 Mar 1992

Kan Y W

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

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

Share to Anemia, Sickle Cell
Share to Chromosome Deletion
Share to DNA
Share to Genetic Therapy

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

Share to Mutation

Share to Polymorphism, Genetic

Share to Thalassemia

Source

Identifiers

PMID: 1538544

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 · 12 closest

Development of DNA analysis for human diseases. Sickle cell anemia and thalassemia as a paradigm.PMID 1538544Read ↗

DNA diagnosis of hemoglobin mutations.Semantic proximity Read ↗

Advances in technologies for screening and diagnosis of hemoglobinopathies.Semantic proximity Read ↗

The future of DNA diagnostics.Semantic proximity Read ↗

The future of DNA diagnostics.Semantic proximity Read ↗

Strategies and applications of DNA level diagnosis in genetic diseases: past experiences and future directions.Semantic proximity Read ↗

[Basics of DNA diagnosis].Semantic proximity Read ↗

Progress in the DNA diagnosis of hemophilias.Semantic proximity Read ↗

Approaches to DNA methods for the detection of heritable mutations in humans.Semantic proximity Read ↗

Genetic diseases of hemoglobin: diagnostic methods for elucidating beta-thalassemia mutations.Semantic proximity Read ↗

[Indications for chromosome and DNA analysis for diagnosis of genetic diseases].Semantic proximity Read ↗

Sickle Cell Trait—Neglected Opportunities in the Era of Genomic MedicineSemantic proximity Read ↗

DNA genotyping.Semantic proximity Read ↗

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