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Publications by C G Mathew
Accurate Diagnosis of Carriers of Deletions and Duplications in Duchenne/Becker Muscular Dystrophy by Fluorescent Dosage Analysis.
Journal of Medical Genetics
Genetics
Clinical, Cytogenetic, and Molecular Analysis of Three Families With FRAXE.
Journal of Medical Genetics
Genetics
Related publications
Improved Diagnosis of Duchenne/Becker Muscular Dystrophy.
Journal of Clinical Investigation
Medicine
Symptomatic Form of Muscular Dystrophy of Duchenne and Becker in Female Carriers
Assessing the Barriers to Cardiac Care in Carriers of Duchenne and Becker Muscular Dystrophy
Journal of Genetic Counseling
Genetics
Comparative Proteomic Analyses of Duchenne Muscular Dystrophy and Becker Muscular Dystrophy Muscles: Changes Contributing to Preserve Muscle Function in Becker Muscular Dystrophy Patients
Journal of Cachexia, Sarcopenia and Muscle
Orthopedics
Sports Medicine
Physiology
Genetic Analysis of 1051 Chinese Families With Duchenne/Becker Muscular Dystrophy
BMC Medical Genetics
Genetics
Analysis of Scottish Duchenne and Becker Muscular Dystrophy Families With Dystrophin cDNA Probes.
Journal of Medical Genetics
Genetics
Impaired Glucose Tolerance in Adults With Duchenne and Becker Muscular Dystrophy
Nutrients
Nutrition
Food Science
Dietetics
Motor Clinical Progression in a Series of Pediatric Duchenne and Becker Muscular Dystrophy Cases
Paediatrica Indonesiana
Malignant Hyperthermia-Like Reactions in Duchenne or Becker Muscular Dystrophy: Review and Hypothesis
Clinical Neurology
Neurology
