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

Benign clinical phenotype of co-inherited congenital dyserythropoietic anaemia type I and heterozygous haemoglobin Lepore.

European journal of haematology - 1 Jul 2023

Li Eric Wenlong, Walsh Rebecca, Ho P Joy

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, Dyserythropoietic, Congenital
Share to Hemoglobins, Abnormal
Share to Heterozygote
Share to Phenotype

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 37037770
DOI: 10.1111/ejh.13974

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

Benign clinical phenotype of co-inherited congenital dyserythropoietic anaemia type I and heterozygous haemoglobin Lepore.PMID 37037770Read ↗

Congenital dyserythropoietic anaemias: clinical features, haematological morphology and new biochemical dataSemantic proximity Read ↗

Congenital dyserythropoietic anemias.Semantic proximity Read ↗

A novel variant mutation for congenital dyserythropoietic anemia, type II.Semantic proximity Read ↗

Benign clinical course in homozygous sickle cell disease: A search for predictorsSemantic proximity Read ↗

The pathogenesis, diagnosis and management of congenital dyserythropoietic anaemia type ISemantic proximity Read ↗

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

Congenital dyserythropoietic anemias: III's a charm.Semantic proximity Read ↗

Congenital dyserythropoietic anaemia type I with nails and bone abnormalities.Semantic proximity Read ↗

Hereditary xerocytosis, a misleading anemia.Semantic proximity Read ↗

Advances in the understanding of the congenital dyserythropoietic anaemias.Semantic proximity Read ↗

Congenital dyserythropoietic anemia type II mimicking hereditary spherocytosis in Indian patient with SEC23B-Y462C mutations.Semantic proximity Read ↗

Hereditary xerocytosis and familial haemolysis due to mutation in the PIEZO1 gene: a simple diagnostic approach.Semantic proximity Read ↗

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