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Article

Use of D11S2179 and D11S1343 as markers for prenatal diagnosis of ataxia telangiectasia in Iranian patients.

Archives of medical research - 1 Oct 2007

Bayat Behnaz, Houshmand Massoud, Sanati Mohammad Hossein, Moin Mostafa, Panahi Mehdi Shafa Shariat, Aleyasin Seyed Ahmad, Isaian Anna, Farhoodi Abolhasan

Abstract excerpt

Ataxia telangiectasia (AT) is an autosomal recessive disorder with an estimated prevalence of 1/40,000 to 1/100,000 in reported populations. There is a 25% possibility for having an affected child when parents are carriers for the ATM gene mutation. There is no cure available for this disease and...

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Source

Identifiers

PMID: 17845903
DOI: 10.1016/j.arcmed.2007.04.008

Genes

ATM

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-17845903-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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Use of D11S2179 and D11S1343 as markers for prenatal diagnosis of ataxia telangiectasia in Iranian patients.PMID 17845903Read ↗

Clinical Characterization and Mutation Analysis of 13 Iranian Ataxia-Telangiectasia Patients: Introducing Three Novel MutationsSemantic proximity Read ↗

Exploration of clinical and genetic findings in Ataxia-Telangiectasia (AT) patients from the Indian subcontinent.Semantic proximity Read ↗

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Health risks for ataxia-telangiectasia mutated heterozygotes: a systematic review, meta-analysis and evidence-based guideline.Semantic proximity Read ↗

Molecular prenatal diagnosis of ataxia telangiectasia heterozygosity by direct mutational assays.Semantic proximity Read ↗

Identification of two mutations for ataxia telangiectasia among the Druze community.Semantic proximity Read ↗

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Management of Individuals With a Mutation in the Ataxia Telangiectasia Mutated Gene.Semantic proximity Read ↗

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