Genetic analysis of 1051 Chinese families with Duchenne/Becker Muscular Dystrophy

Prenatal diagnosis of Duchenne muscular dystrophy in 131 Chinese families with dystrophinopathy

(2017) Huanhuan Wang et al.   PRENATAL DIAGNOSIS

Next-generation sequencing in neuromuscular diseases

(2016) Stephanie Efthymiou et al.   CURRENT OPINION IN NEUROLOGY

Genetic diagnosis of Duchenne/Becker muscular dystrophy using next-generation sequencing: validation analysis of DMD mutations

(2016) Mariko Okubo et al.   JOURNAL OF HUMAN GENETICS

The TREAT-NMD DMD Global Database: Analysis of More than 7,000 Duchenne Muscular Dystrophy Mutations

(2015) Catherine L. Bladen et al.   HUMAN MUTATION

A systematic review and meta-analysis on the epidemiology of Duchenne and Becker muscular dystrophy

(2014) Jean K. Mah et al.   NEUROMUSCULAR DISORDERS

Xp21/A Translocation: A Rarely Considered Genetic Cause for Manifesting Carriers of Duchenne Muscular Dystrophy

(2014) Stefan Wieczorek et al.   NEUROPEDIATRICS

Newborn bloodspot screening for Duchenne Muscular Dystrophy: 21 years experience in Wales (UK)

(2013) Stuart J Moat et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Genetic characterization in symptomatic female DMD carriers: lack of relationship between X-inactivation, transcriptional DMD allele balancing and phenotype

(2012) Simona Brioschi et al.   BMC Medical Genetics

Combination of conventional multiplex PCR and quantitative real-time PCR detects large rearrangements in the dystrophin gene in 59% of Syrian DMD/BMD patients

(2010) Ammar Madania et al.   CLINICAL BIOCHEMISTRY

Empirical Evaluation of Oligonucleotide Probe Selection for DNA Microarrays

(2010) Jennifer G. Mulle et al.   PLoS One

Homozygous female Becker muscular dystrophy

(2009) Katsunori Fujii et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management

(2009) Katharine Bushby et al.   LANCET NEUROLOGY