Incidental findings on array comparative genomic hybridization: detection of carrier females of dystrophinopathy without any family history

Genetic and clinical specificity of 26 symptomatic carriers for dystrophinopathies at pediatric age

(2013) Sandra Mercier et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Assessing Pathogenicity for Novel Mutation/Sequence Variants: The Value of Healthy Older Individuals

(2012) Mayana Zatz et al.   NEUROMOLECULAR MEDICINE

Unexpected findings in cancer predisposition genes detected by array comparative genomic hybridisation: what are the issues?

(2011) G. Pichert et al.   JOURNAL OF MEDICAL GENETICS

Unexpected detection of dystrophin gene deletions by array comparative genomic hybridization

(2010) Catherine E. Cottrell et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Infantile Convulsions with Paroxysmal Dyskinesia (ICCA Syndrome) and Copy Number Variation at Human Chromosome 16p11

(2010) Patrice Roll et al.   PLoS One

Genotype-phenotype analysis in 2,405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase

(2009) Sylvie Tuffery-Giraud et al.   HUMAN MUTATION

Molecular diagnosis of Duchenne/Becker muscular dystrophy: enhanced detection of dystrophin gene rearrangements by oligonucleotide array-comparative genomic hybridization

(2008) Daniela del Gaudio et al.   HUMAN MUTATION

Microarray-based mutation detection in thedystrophingene

(2008) Madhuri R. Hegde et al.   HUMAN MUTATION