Detection of subclinical and carrier states in Duchenne muscular dystrophy
- 1 July 1966
- journal article
- research article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 69 (1) , 67-79
- https://doi.org/10.1016/s0022-3476(66)80363-3
Abstract
No abstract availableThis publication has 32 references indexed in Scilit:
- Muscular Dystrophy (Duchenne) in a Girl with Turner's SyndromeJournal of Medical Genetics, 1965
- Muscle Histology in Carriers of Duchenne Muscular DystrophyJournal of Medical Genetics, 1965
- Electromyography in pediatric neuromuscular disordersThe Journal of Pediatrics, 1965
- THE USE OF LEAD CITRATE AT HIGH pH AS AN ELECTRON-OPAQUE STAIN IN ELECTRON MICROSCOPYThe Journal of cell biology, 1963
- CLINICAL, GENETIC AND ELECTROCARDIOGRAPHIC STUDIES IN CHILDHOOD MUSCULAR DYSTROPHYThe Lancet Healthy Longevity, 1961
- Gene Action in the X-chromosome of the Mouse (Mus musculus L.)Nature, 1961
- MUSCULAR DYSTROPHY IN CHILDHOOD. THE GENETIC ASPECT.Annals of Human Genetics, 1958
- THE PROGNOSTIC VALUE OF THE MUSCLE BIOPSY IN THE “FLOPPY INFANT”Brain, 1958
- AUTOSOMAL RECESSIVE INHERITANCE OF DUCHENNE‐TYPE MUSCULAR DYSTROPHYAnnals of Human Genetics, 1957
- ELECTROMYOGRAPHY IN MUSCULAR DYSTROPHIES: DIFFERENTIATION BETWEEN DYSTROPHIES AND CHRONIC LOWER MOTOR NEURONE LESIONSJournal of Neurology, Neurosurgery & Psychiatry, 1949