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

Detection of nine Mediterranean β-thalassemia mutations in Palestinians using three restriction enzyme digest panels: a reliable method for developing countries.

Hemoglobin - 1 Jan 2014

Reading N Scott, Sirdah Mahmoud M, Tarazi Issa S, Prchal Josef T

Abstract excerpt

β-Thalassemia (β-thal) is a public health problem in the Gaza Strip, Palestine, where about 320 patients are currently managed through blood transfusions and iron chelation. Within the restrictive environment of the Gaza Strip, no advanced molecular analysis [sequencing, real-time polymerase chain reaction (real-time PCR)] technology is currently available for developing a premarital screening protocol and...

Read the complete abstract on PubMed

Topics

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

Share to Amplified Fragment Length Polymorphism Analysis
Share to Arabs

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

Share to beta-Globins

Share to beta-Thalassemia

Share to Developing Countries

Share to DNA Restriction Enzymes

Share to Mutation

Share to Reproducibility of Results

Source

Identifiers

PMID: 24144202
DOI: 10.3109/03630269.2013.845105

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

Detection of nine Mediterranean β-thalassemia mutations in Palestinians using three restriction enzyme digest panels: a reliable method for developing countries.PMID 24144202Read ↗

The spectrum of β-thalassemia mutations in Gaza Strip, Palestine.Semantic proximity Read ↗

Spectrum of beta-globin gene mutations among thalassemia patients in the West Bank region of Palestine.Semantic proximity Read ↗

Scanning of beta-globin gene for identification of beta-thalassemia mutation in Romanian population.Semantic proximity Read ↗

Detection of eight beta-thalassemia mutations using a DNA enzyme immunoassay.Semantic proximity Read ↗

Accurate and rapid prenatal diagnosis of the most frequent East Mediterranean beta-thalassemia mutations.Semantic proximity Read ↗

New Insights on β-Thalassemia in the Palestinian Population of Gaza: High Frequency and Milder Phenotype Among Homozygous IVS-I-1 (HBB: c.92+1G>A) Patients with High Levels of Hb F.Semantic proximity Read ↗

Molecular heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Gaza Strip Palestinians.Semantic proximity Read ↗

Rapid screening of multiple beta-globin gene mutations by real-time PCR on the LightCycler: application to carrier screening and prenatal diagnosis of thalassemia syndromes.Semantic proximity Read ↗

Molecular Understanding of Severe Cases of β-Thalassemia in the Nablus Region, West Bank, Palestine.Semantic proximity Read ↗

Rapid diagnosis of beta thalassemia mutations in Mediterraneans by PCR and restriction analysis of natural or created sites.Semantic proximity Read ↗

Rapid detection of fetal Mendelian disorders: thalassemia and sickle cell syndromes.Semantic proximity Read ↗

Hemolysis and Mediterranean G6PD mutation (c.563 C>T) and c.1311 C>T polymorphism among Palestinians at Gaza Strip.Semantic proximity Read ↗

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