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 Laboratory Manifestation and Molecular Diagnosis of β-Thalassemia Patients in Iraq.

Journal of pediatric hematology/oncology - 1 Jan 2020

AlMosawi Riham H N, Al-Rashedi Nihad A M, Ayoub Najla I

Abstract excerpt

Many studies determined the demographic and ethnic border of patients with beta (β)-thalassemia mutations and their migration. The effective way to health care policy of β-thalassemia is to prevent homozygote births and reduce the severity of the disease. The objectives of this study contributed to investigating the molecular and serologic characteristics of β-thalassemia patients in Iraq. Peripheral blood...

Read the complete abstract on PubMed

Topics

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

Share to 8-Hydroxy-2'-Deoxyguanosine
Share to beta-Globins
Share to beta-Thalassemia

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

Share to Calcifediol

Share to Ferritins

Share to Molecular Diagnostic Techniques

Share to Sequence Deletion

Source

Identifiers

PMID: 31714438
DOI: 10.1097/MPH.0000000000001656

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. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical Laboratory Manifestation and Molecular Diagnosis of β-Thalassemia Patients in Iraq.PMID 31714438Read ↗

Genetic variations and clinical implications of B-thalassemia in Iraqi population.Semantic proximity Read ↗

Genotype-Phenotype Correlation of Β-Globin Mutations and Hematological Parameters in Iraqi Β-Thalassemia Patients.Semantic proximity Read ↗

Prevalence and Molecular Characterization of β-Thalassemia in Kirkuk Province of Northern Iraq.Semantic proximity Read ↗

β-THALASSEMIA IN TURKEY: A REVIEW OF THE CLINICAL, EPIDEMIOLOGICAL, MOLECULAR, AND EVOLUTIONARY ASPECTSSemantic proximity Read ↗

Identification of novel mutations in β-thalassemia patients in Maysan Governorate, Iraq.Semantic proximity Read ↗

Genetic Epidemiology, Hematological and Clinical Features of Hemoglobinopathies in IranSemantic proximity Read ↗

Recent progress in laboratory diagnosis of thalassemia and hemoglobinopathy: a study by the Korean Red Blood Cell Disorder Working Party of the Korean Society of HematologySemantic proximity Read ↗

Genetic epidemiology of beta-thalassemia in the Maldives: 23 years of a beta-thalassemia screening program.Semantic proximity Read ↗

Update in Laboratory Diagnosis of ThalassemiaSemantic proximity Read ↗

Epidemiology and treatment of beta thalassemia major in ChinaSemantic proximity Read ↗

Molecular Basis of β-Thalassemia in the Population of the Aegean Region of Turkey: Identification of A Novel Deletion Mutation.Semantic proximity Read ↗

Molecular analysis of alpha- and beta-thalassemia in Meizhou region and comparison of gene mutation spectrum with different regions of southern China.Semantic proximity Read ↗

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