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

Clinical and molecular characterization of β(S) and (G)γ((A)γδβ)⁰-thalassemia in eastern India.

Hemoglobin - 1 Jan 2010

Patel Dilip Kumar, Patel Madhumita, Mashon Ranjeet Singh, Patel Siris, Dash Preetinanda Manaswini, Das Bhabani Shankar

Abstract excerpt

Fetal hemoglobin (Hb F) is the most studied modifier of sickle cell disease. Coinheritance of high Hb F determinants such as δβ-thalassemia (δβ-thal) and hereditary persistence of fetal hemoglobin (HPFH) can contribute to raised Hb F concentration in these patients. One hundred and seventy-six ca...

Read the complete abstract on PubMed

Topics

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

Share to Anemia, Sickle Cell
Share to beta-Thalassemia
Share to Child

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Fetal Hemoglobin

Share to Genetic Association Studies

Share to Heterozygote

Share to Young Adult

Source

Identifiers

PMID: 21077771
DOI: 10.3109/03630269.2010.526890

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-21077771-2026-09-02.2. 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

Clinical and molecular characterization of β(S) and (G)γ((A)γδβ)⁰-thalassemia in eastern India.PMID 21077771Read ↗

Contrasting co-inheritance of alpha and beta mutations in delta beta thalassemia and hereditary persistence of fetal hemoglobin: a study from India.Semantic proximity Read ↗

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

Prevalence and molecular characterization of alpha-thalassemia syndromes among Indians.Semantic proximity Read ↗

Beta-thalassemias: expression, molecular mechanisms and mutations in Indians.Semantic proximity Read ↗

Genetic Basis and Genetic Modifiers of β-Thalassemia and Sickle Cell Disease.Semantic proximity Read ↗

Clinical, hematologic and molecular variability of sickle cell-β thalassemia in western IndiaSemantic proximity Read ↗

Phenotypic expression of Hb F in common high Hb F determinants in Thailand: roles of α-thalassemia, 5' δ-globin BCL11A binding region and 3' β-globin enhancer.Semantic proximity Read ↗

A large cohort of deletional high hemoglobin F determinants in Thailand: A molecular revisited and identification of a novel mutation.Semantic proximity Read ↗

Inherited hemoglobin disorders in Andhra Pradesh, India: a population study.Semantic proximity Read ↗

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

Prevalence of the β(S) gene among scheduled castes, scheduled tribes and other backward class groups in Central India.Semantic proximity Read ↗

Genetic association studies in β-hemoglobinopathiesSemantic proximity Read ↗

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