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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 mu...

Topics

DNA Probes
Female
Fetal Diseases
Gene Deletion
Humans
Male
Muscular Dystrophies
Mutation
Polymerase Chain Reaction
Pregnancy
Prenatal Diagnosis

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 8001417

Genes

DMD

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-8001417-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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

[Study on Duchenne muscular dystrophy gene mutation and prenatal diagnosis].Semantic proximity Read ↗

[Clinical value of MLPA in the prenatal gene diagnosis of Duchenne muscular dystrophy].Semantic proximity Read ↗

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[Analysis of results of prenatal diagnosis for 67 pedigrees affected with Duchenne muscular dystrophy in the central plain region of China].Semantic proximity Read ↗

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

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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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