Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

[Genetic diagnosis of Duchenne/Becker muscular dystrophy by MLPA].

Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics - 1 Jun 2014

Zhang Yuanyuan, Liu Xiaoliang, He Rong, Ma Hongwei, Zhao Yanyan

Abstract excerpt

OBJECTIVE: To assess the value of multiplex ligation-dependent probe amplification (MLPA) for the genetic and prenatal diagnosis of Duchenne/Becker muscular dystrophy (DMD/BMD). METHODS: Forty seven patients clinically diagnosed or suspected with DMD/BMD were recruited. Deletion or duplication of the 79 exons of the DMD gene were detected by MLPA. PCR and sequencing were used to detect single exon deletion. MLPA...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Fetal Diseases
Share to Gene Deletion

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Genetic Testing

Share to Infant, Newborn

Share to Multiplex Polymerase Chain Reaction

Share to Muscular Dystrophy, Duchenne

Share to Pregnancy

Share to Prenatal Diagnosis

Source

Identifiers

PMID: 24928015
DOI: 10.3760/cma.j.issn.1003-9406.2014.03.018

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Genetic diagnosis of Duchenne/Becker muscular dystrophy by MLPA].PMID 24928015Read ↗

[Mutation analysis and prenatal diagnosis of families affected with Duchenne and Becker muscular dystrophy].Semantic proximity Read ↗

[Prenatal diagnosis of Duchenne and Becker muscular dystrophy by multiplex ligation-dependent probe amplification].Semantic proximity Read ↗

[Detection of genomic duplications and deletions of the DMD gene in affected males and female carriers by using mutiplex ligation-dependent probe amplification].Semantic proximity Read ↗

[Genotype, phenotype analysis and follow-up study on patients with Duchenne/Becker muscular dystrophy].Semantic proximity Read ↗

[Detection of mutations causing Duchenne and Becker muscular dystrophies: multiplex polymerase chain reaction vs. Multiplex ligation dependent probe amplification].Semantic proximity Read ↗

[Detection of rare mutations in the dystrophin gene].Semantic proximity Read ↗

Genetic analysis of the dystrophin gene in children with Duchenne and Becker muscular dystrophies.Semantic proximity Read ↗

[Mutation analysis of 81 cases with Duchenne/Becker muscular dystrophy].Semantic proximity Read ↗

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

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

[Identification of deletion/duplication mutations in DMD gene by multiple ligation probe amplification and denaturing high-performance liquid chromatography].Semantic proximity Read ↗

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

⌁Select a neighboring publication to make it the new centre.