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[Carrier detection and prenatal diagnosis of Duchenne's muscular dystrophy based on DNA analysis].

Zhurnal nevropatologii i psikhiatrii imeni S.S. Korsakova (Moscow, Russia : 1952) - 1 Jan 1990

Evgrafov O V, Badalian L O, Poliakov A V, Zaĭtseva S P, Malygina N A, Vinogradov S V, Bakharev V A, Mil'man F A, Lisova L P, Zaretskaia N V

Abstract excerpt

Seven families with histories of Duchenne's muscular dystrophy underwent DNA diagnosis. The daughters of those consulted were examined for the carriage in 4 families. Their carriage was rejected or confirmed. Prenatal diagnosis was made in 2 families. In another family an abortion preceded obtaining molecular-genetic evidence. Probes 754, p20, XJI.I and primers for amplification of the site pERI87-15 containing a...

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PMID: 2175114

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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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