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Article

Carrier detection in Duchenne and Becker muscular dystrophy Argentine families.

Clinical genetics - 1 Dec 1998

Baranzini S E, Giliberto F, Dalamon V, Barreiro C, García-Erro M, Grippo J, Szijan I

Abstract excerpt

In order to offer carrier detection, genetic counseling, and prenatal diagnosis to families with Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) in our country, segregation analysis of highly polymorphic short tandem repeats (STR) (dC-dA)n: (dG-dT)n loci was utilized. The risks to females of 15 DMD BMD families (9 familial and 6 sporadic) were evaluated on STR, pedigree and serum creatine...

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Source

Identifiers

PMID: 9894797
DOI: 10.1111/j.1399-0004.1998.tb03771.x

Genes

DMD

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.

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