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Article

Gene diagnosis for nine Chinese patients with DMD/BMD by multiplex ligation-dependent probe amplification and prenatal diagnosis for one of them.

Journal of clinical laboratory analysis - 1 Jan 2009

Wu Yupeng, Yin Gengxin, Fu Keqin, Wu De, Zhai Qian, Du Huarong, Huang Zhongjun, Niu Yuhua

Abstract excerpt

This study aims to perform gene diagnosis for nine patients with Duchenne/Becker muscular dystrophy (DMD/BMD) and their parents with multiplex ligation-dependent probe amplification (MLPA), and to carry out prenatal gene diagnosis for one of them. Genomic DNA of the peripheral blood and fetal amniotic fluid cell was extracted from the pedigrees' members with DMD/BMD. Gene diagnosis was performed for theses...

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Share to Amniotic Fluid
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Muscular Dystrophy, Duchenne

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Source

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Identifiers

PMID: 19927354
DOI: 10.1002/jcla.20349
PMCID: PMC6649174

Genes

DMD
KIT

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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