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

Wide range of F cell levels in healthy Thai adults: Influence of Swiss-type hereditary persistence of foetal haemoglobin & β-haemoglobinopathy.

The Indian journal of medical research - 1 Aug 2019

Tatu Thanusak

Abstract excerpt

Background & objectives: Swiss-type hereditary persistence of foetal haemoglobin (HPFH) has been shown to be responsible for the wide range of F cell levels in healthy Thai adults. However, a survey for F cells in healthy Thai adults has not been performed. This study was conducted to determine the F cell distribution in adult Thai blood donors and to assess the possible involvement of β-thalassaemia and...

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 Blood Donors

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Erythrocyte Indices

Share to Fetal Hemoglobin

Share to Hemoglobin E

Share to Hemoglobinopathies

Share to Thailand

Source

Open in PubMed Open full text

Identifiers

PMID: 31670271
DOI: 10.4103/ijmr.IJMR_1954_17
PMCID: PMC6829780

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Wide range of F cell levels in healthy Thai adults: Influence of Swiss-type hereditary persistence of foetal haemoglobin & β-haemoglobinopathy.PMID 31670271Read ↗

[Genetically based states of elevated quantity of foetal haemoglobin (Hb F) in healthy individuals and patients].Semantic 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 ↗

Molecular basis and hematologic characterization of deltabeta-thalassemia and hereditary persistence of fetal hemoglobin in Thailand.Semantic proximity Read ↗

Foetal Haemoglobin, Erythrocytes Containing Foetal Haemoglobin, and Hematological Features in Congolese Patients with Sickle Cell AnaemiaSemantic proximity Read ↗

Effect of Swiss-type heterocellular HPFH from XmnI-Gγ and HBBP1 polymorphisms on HbF, HbE, MCV and MCH levels in Thai HbE carriers.Semantic proximity Read ↗

The role of heterocellular hereditary persistence of fetal haemoglobin in beta(0)-thalassaemia intermedia.Semantic proximity Read ↗

Hereditary persistence of hemoglobin F is protective against red cell sickling. A case report and brief reviewSemantic proximity Read ↗

Fetal haemoglobin levels and haematological characteristics of compound heterozygotes for haemoglobin S and deletional hereditary persistence of fetal haemoglobinSemantic proximity Read ↗

Heterocellular hereditary persistence of fetal haemoglobin affects the haematological parameters of beta-thalassaemia trait.Semantic proximity Read ↗

Haemoglobin F levels in healthy Nigerian adults.Semantic proximity Read ↗

Genetics of Hb F/F cell variance in adults and heterocellular hereditary persistence of fetal hemoglobin.Semantic proximity Read ↗

A new type of hereditary persistence of fetal haemoglobin (HPFH): HPFH Tunisia beta + (+C-200)G gamma.Semantic proximity Read ↗

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