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

Compound heterozygosity for HbD Punjab and polyadenylation signal mutation causes clinically asymptomatic mild hypochromia and microcytosis.

Annals of hematology - 1 Jun 2010

Girisha Katta Mohan, Vahab Saadi Abdul, Dalal Ashwin B, Gopinath P M, Satyamoorthy K

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, Hypochromic
Share to DNA Mutational Analysis
Share to Genetic Counseling
Share to Hematologic Diseases

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

Share to Hemoglobins, Abnormal

Share to Heterozygote

Share to Infant

Share to Severity of Illness Index

Source

Identifiers

PMID: 19727721
DOI: 10.1007/s00277-009-0827-2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 16 Oct 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

Compound heterozygosity for HbD Punjab and polyadenylation signal mutation causes clinically asymptomatic mild hypochromia and microcytosis.PMID 19727721Read ↗

A novel splice site mutation in the ADAR gene leading to exon skipping and dyschromatosis symmetrica hereditaria in a Japanese patient.Semantic proximity Read ↗

Nomenclature for human DPYD alleles.Semantic proximity Read ↗

Hemoglobin D-Punjab: origin, distribution and laboratory diagnosisSemantic proximity Read ↗

Mild Hb S-beta(+)-thalassemia with a deletion of five nucleotides at the polyadenylation site of the beta-globin gene.Semantic proximity Read ↗

Dyschromatosis Symmetrica Hereditaria and Aicardi-Goutières Syndrome 6 Are Phenotypic Variants Caused by ADAR1 Mutations.Semantic proximity Read ↗

Novel de novo heterozygous frameshift mutation of the ADAR1 gene in heavy dyschromatosis symmetrica hereditaria.Semantic proximity Read ↗

ADAR1 splicing mutation leading to dyschromatosis hereditaria in a Caucasian patient.Semantic proximity Read ↗

Pathogenicity of ADAR1 mutation in a Chinese family with dyschromatosis symmetrica hereditaria.Semantic proximity Read ↗

Coexistence of rare variant HbD Punjab [α2β2(121(Glu→Gln))] and alpha 3.7 kb deletion in a young boy of Hindu family in West Bengal, India.Semantic proximity Read ↗

Lost in translation: RP and GATA1 mutations in DBA.Semantic proximity Read ↗

[Autosomal-recessive amylosis cutis dyschromica and GPNMB mutations].Semantic proximity Read ↗

Two novel splice site mutations of the ADAR1 gene in Chinese families with dyschromatosis symmetrica hereditaria.Semantic proximity Read ↗

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