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

Erythrocytosis and the Chuvash von Hippel-Lindau mutation.

British journal of haematology - 1 Oct 2003

Percy Melanie J, Beard Michael E J, Carter Chris, Thein Swee Lay

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 Follow-Up Studies
Share to Infant
Share to Ligases
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Polycythemia

Share to Tumor Suppressor Proteins

Share to Ubiquitin-Protein Ligases

Share to Von Hippel-Lindau Tumor Suppressor Protein

Source

Identifiers

PMID: 14531927
DOI: 10.1046/j.1365-2141.2003.04631.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Erythrocytosis and the Chuvash von Hippel-Lindau mutation.PMID 14531927Read ↗

Von hippel-lindau disease and erythrocytosis.Semantic proximity Read ↗

Erythrocytosis: genes and pathways involved in disease development.Semantic proximity Read ↗

Genetically heterogeneous origins of idiopathic erythrocytosis.Semantic proximity Read ↗

JAK2 wild-type erythrocytosis: concept, differential diagnosis, diagnostic steps, and treatment approaches.Semantic proximity Read ↗

Molecular study of congenital erythrocytosis in 70 unrelated patients revealed a potential causal mutation in less than half of the cases (Where is/are the missing gene(s)?).Semantic proximity Read ↗

Erythroleukemia-historical perspectives and recent advances in diagnosis and managementSemantic proximity Read ↗

Congenital erythrocytosis.Semantic proximity Read ↗

Familial erythrocytosis 2 and von Hippel-Lindau disease in the same pediatric patient.Semantic proximity Read ↗

Chuvash polycythemia: diagnosis and management.Semantic proximity Read ↗

Genetic Background of Congenital Erythrocytosis.Semantic proximity Read ↗

Genetic mutations and abnormal hemoglobins.Semantic proximity Read ↗

The Kell blood group system and the McLeod phenotype.Semantic proximity Read ↗

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