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  1. Symptomatic female carriers of Duchenne muscular dystrophy (DMD): Genetic and clinical characterization
  2. Molecular diagnosis of dystrophinopathies using a multi-technique analysis algorithm
  3. Spectrum ofRB1Mutations in Argentine Patients: 20-years Experience in the Molecular Diagnosis of Retinoblastoma
  4. Prenatal diagnosis of duchenne/becker muscular dystrophy by short tandem repeat segregation analysis in argentine families
  5. Neurofibromatosis type 2: Molecular and clinical analyses in Argentine sporadic and familial cases
  6. Carrier detection in Duchenne and Becker muscular dystrophy Argentine families
  7. Detection of deletions and duplications in the Duchenne muscular dystrophy gene by the molecular method MLPA in the first Argentine affected families
  8. The Role of Polymorphic Short Tandem (CA)n Repeat Loci Segregation Analysis in the Detection of Duchenne Muscular Dystrophy Carriers and Prenatal Diagnosis
  9. The Role of Polymorphic Short Tandem (CA)n Repeat Loci Segregation Analysis in the Detection of Duchenne Muscular Dystrophy Carriers and Prenatal Diagnosis
  10. Detection of germline mosaicism in two duchenne muscular dystrophy families using polymorphic dinucleotide (CA)n repeat loci within the dystrophin gene
  11. Dystrophin deletions and cognitive impairment in Duchenne/Becker muscular dystrophy
  12. Detection of Germline Mosaicism in Two Duchenne Muscular Dystrophy Families Using Polymorphic Dinucleotide (CA)n Repeat Loci Within the Dystrophin Gene
  13. Clinical, cytogenetic, and molecular testing of Argentine patients with retinoblastoma