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

Access to a syllabus of human hemoglobin variants (1996) via the World Wide Web.

Hemoglobin - 1 Mar 1998

Hardison R C, Chui D H, Riemer C R, Miller W, Carver M F, Molchanova T P, Efremov G D, Huisman T H

Abstract excerpt

Information on mutations in human hemoglobin is important in many efforts, including understanding the pathophysiology of hemoglobin diseases, developing therapies, elucidating the dynamics of sequence alterations inhuman populations, and dissecting the details of protein structure/function relationships. Currently, information is available on a large number of mutations and variants, but is distributed among...

Read the complete abstract on PubMed

Topics

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

Share to Computer Communication Networks
Share to Databases, Factual

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

Share to Genetic Variation

Share to Globins

Share to Hemoglobinopathies

Share to Hemoglobins, Abnormal

Share to Point Mutation

Source

Identifiers

PMID: 9576329
DOI: 10.3109/03630269809092136

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

Access to a syllabus of human hemoglobin variants (1996) via the World Wide Web.PMID 9576329Read ↗

Databases of human hemoglobin variants and other resources at the globin gene server.Semantic proximity Read ↗

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

HbVar: A relational database of human hemoglobin variants and thalassemia mutations at the globin gene server.Semantic proximity Read ↗

HbVar database of human hemoglobin variants and thalassemia mutations: 2007 update.Semantic proximity Read ↗

Improvements in the HbVar database of human hemoglobin variants and thalassemia mutations for population and sequence variation studies.Semantic proximity Read ↗

International Hemoglobin Information Center. Variant list.Semantic proximity Read ↗

Clinically relevant updates of the HbVar database of human hemoglobin variants and thalassemia mutations.Semantic proximity Read ↗

Updates of the HbVar database of human hemoglobin variants and thalassemia mutations.Semantic proximity Read ↗

International Hemoglobin Information Center variants list.Semantic proximity Read ↗

Classification of the disorders of hemoglobin.Semantic proximity Read ↗

LOVD–DASH: A comprehensive LOVD database coupled with diagnosis and an at‐risk assessment system for hemoglobinopathiesSemantic proximity Read ↗

Genetic mutations and abnormal hemoglobins.Semantic proximity Read ↗

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