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Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Book Review : The History of a Genetic Disease: Duchenne Muscular Dystrophy or Meryon’s DiseaseDOI 10.1017/mdh.2012.7
The history of a genetic disease: Duchenne muscular dystrophy or Meryon's diseaseSemantic proximity
Authors muscle in on history: The History of a Genetic Disease Duchenne Muscular Dystrophy or Meryon's diseaseSemantic proximity
[Duchenne's muscular dystrophy: epidemiology, genetics, diagnosis].Semantic proximity
Neurofibromatosis: Phenotype, Natural History and PathogenesisSemantic proximity
Changing clinical concepts of Duchenne muscular dystrophy: molecular genetic diagnosis.Semantic proximity
Gene table of monogenic neuromuscular disorders (nuclear genome only) Vol. 18 No. 1, January 2008.Semantic proximity
Genetic Disorders and the Fetus. Diagnosis, Prevention and TreatmentSemantic proximity
[Genetic aspects of muscular diseases].Semantic proximity
Book Review : A century of Mendelism in human genetics: proceedings of a symposium organised by the Galton Institute and held at the Royal Society of Medicine, London, 2001Semantic proximity
The 2016 version of the gene table of monogenic neuromuscular disorders (nuclear genome)Semantic proximity
The 2014 version of the gene table of monogenic neuromuscular disorders (nuclear genome)Semantic proximity
Novel human pathological mutations. Gene symbol: DMD. Disease: muscular dystrophy, Duchenne.Semantic proximity
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