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

Molecular diversity of hemoglobin H disease in India.

American journal of clinical pathology - 1 Mar 2010

Nadkarni Anita H, Nair Sona B, Italia Khushnooma Y, Warang Prashant, Dalvi Madhura, Ghosh Kanjaksha, Colah Roshan B

Abstract excerpt

This study was undertaken to evaluate the variable clinical expression of hemoglobin (Hb) H disease in India. For the study, alpha genotyping was done in 8 patients with Hb H disease using multiplex polymerase chain reaction and DNA sequencing. The study revealed that 4 genotypes (- -(SEA)/ -alph...

Read the complete abstract on PubMed

Topics

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

Share to SEA gene
Share to Genotype
Share to India

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Mutation

Share to alpha-Thalassemia

Share to Child, Preschool

Share to Polymerase Chain Reaction

Source

Identifiers

PMID: 20154289
DOI: 10.1309/AJCP70ORBRURVSJM

Genes

SEA

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20154289-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Molecular diversity of hemoglobin H disease in India.PMID 20154289Read ↗

The phenotypic and molecular diversity of hemoglobinopathies in India: A review of 15 years at a referral centerSemantic proximity Read ↗

Wide spectrum of novel and rare hemoglobin variants in the multi-ethnic Indian population: A review.Semantic proximity Read ↗

Clinical and genetic characteristics of hemoglobin H disease in Iran.Semantic proximity Read ↗

Genotype-phenotype correlation in Iranian patients with Hb H disease.Semantic proximity Read ↗

Variable clinical phenotypes of alpha-thalassemia syndromes.Semantic proximity Read ↗

Haemoglobinopathies in tribal populations of IndiaSemantic proximity Read ↗

Molecular spectrum of Hb H disease and characterization of rare deletional α-thalassemia found in ThailandSemantic proximity Read ↗

Hemoglobinopathy in India.Semantic proximity Read ↗

Clinical and molecular analysis of haemoglobin H disease in Sardinia: haematological, obstetric and cardiac aspects in patients with different genotypes.Semantic proximity Read ↗

Epidemiology, Population Health Genetics and Phenotypic Diversity of Sickle Cell Disease in IndiaSemantic proximity Read ↗

[Clinical phenotype genotype correlation in children with hemoglobin H disease in Zhuhai area of China].Semantic proximity Read ↗

Variable presentation of HB H disease due to homozygosity for the rare polyadenylation signal A T(Indian) (AATAAA>AATA- -) mutation in four Indian families.Semantic proximity Read ↗

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