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Article

[Prenatal diagnosis of Duchenne's muscular dystrophy fetus at risk].

Zhonghua fu chan ke za zhi - 1 Jul 1994

Hua X Y, Xu M H, Lin Q D

Abstract excerpt

Prenatal diagnosis of Duchenne's muscular dystrophy (DMD) have been carried out on 12 fetus at risk. The gene mutations have been identified by hybridization with cDNA probes and/or multiplex PCR. The fetus examined were 7 males and 3 females. Three of the male fetus inherited the same deleted mutations as the probands, and other 4 appeared normal. Among the 3 female fetus, one carried a deleted gene, two were...

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Source

Identifiers

PMID: 8001417

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.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

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[Prenatal diagnosis of Duchenne's muscular dystrophy fetus at risk].PMID 8001417Read ↗

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[Molecular-genetic characteristics of mutations in dystrophin gene and clinical symptoms in Duchenne muscular dystrophy].Semantic proximity Read ↗

[Mutation analysis and prenatal diagnosis for 50 pedigrees affected with Duchenne/Becker muscular dystrophy].Semantic proximity Read ↗

Gestational Outcomes of Pregnant Women Who Have Had Invasive Prenatal Testing for the Prenatal Diagnosis of Duchenne Muscular Dystrophy.Semantic proximity Read ↗

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Prenatal diagnosis for a Chinese family with a de novo DMD gene mutation: A case report.Semantic proximity Read ↗

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