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 basis and prenatal diagnosis of β-thalassemia among Balouch population in Iran.

Prenatal diagnosis - 1 Aug 2011

Miri-Moghaddam E, Zadeh-Vakili A, Rouhani Z, Naderi M, Eshghi P, Khazaei Feizabad A

Abstract excerpt

OBJECTIVE: To determine the molecular spectrum of β-thalassemia mutations among at-risk Balouch couples in Iran. METHODS: Mutations' detection in DNAs extracted from the blood of partners of at-risk couples was characterized, and chorion villus sampling by amplification refractory mutation system and DNA sequencing was performed. Fetal diagnosis was also confirmed by linkage analysis. RESULTS: Out of a total of...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to beta-Thalassemia
Share to Consanguinity

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Mutational Analysis

Share to Mutation

Share to Prenatal Diagnosis

Share to Young Adult

Source

Identifiers

PMID: 21692087
DOI: 10.1002/pd.2767

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

Molecular basis and prenatal diagnosis of β-thalassemia among Balouch population in Iran.PMID 21692087Read ↗

Sistani population: a different spectrum of β-thalassemia mutations from other ethnic groups of Iran.Semantic proximity Read ↗

Prenatal screening for β-thalassemia major reveals new and rare mutations in the Pakistani population.Semantic proximity Read ↗

Profile of β-thalassemia and its prenatal diagnosis in Khorasan-e-Jonobi Province, Iran.Semantic proximity Read ↗

Prevalence and Molecular Spectrum of α- and β-Globin Gene Mutations in Hainan, ChinaSemantic proximity Read ↗

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

[A study on gene mutation spectrums of α- and β-thalassemias in populations of Yunnan Province and the prenatal gene diagnosis].Semantic proximity Read ↗

Molecular epidemiology of β-thalassemia in pakistan: Far reaching implicationsSemantic proximity Read ↗

Characterizing a cohort of α-thalassemia couples collected during screening for hemoglobinopathies: 14 years of an Iranian experience.Semantic proximity Read ↗

Mutations in Thalassemia Carrier Couples: The Importance of Prenatal Diagnostic Tests.Semantic proximity Read ↗

Evaluation of α-Globin Gene Mutations Among Different Ethnic Groups in Khuzestan Province, Southwest Iran.Semantic proximity Read ↗

Prevalence and molecular spectrum of α- and β-globin gene mutations in Hainan, China.Semantic proximity Read ↗

Update on Prevention of Hemoglobinopathies in Azerbaijan.Semantic proximity Read ↗

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