Genetic counseling in duchenne muscular dystrophy
- 1 September 1979
- journal article
- Published by Wiley in Muscle & Nerve
- Vol. 2 (5) , 325-328
- https://doi.org/10.1002/mus.880020502
Abstract
No abstract availableThis publication has 45 references indexed in Scilit:
- Serum creatine kinase and pyruvate kinase in duchenne muscular dystrophy carrier detectionMuscle & Nerve, 1979
- Lymphocyte Capping in Duchenne Muscular DystrophyNew England Journal of Medicine, 1979
- CARRIER DETECTION IN DUCHENNE MUSCULAR DYSTROPHY: ASSESSMENT OF THE EFFECT OF AGE ON DETECTION-RATE WITH SERUM-CREATINE-KINASE-ACTIVITYThe Lancet, 1979
- Prenatal Genetic Diagnosis in 3000 AmniocentesesNew England Journal of Medicine, 1979
- Prenatal Diagnosis of Duchenne's Muscular DystrophyNew England Journal of Medicine, 1977
- A possible role for electron microscopy in detection of carriers of Duchenne type muscular dystrophyJournal of Neurology, Neurosurgery & Psychiatry, 1973
- Quantitative electromyography: carrier detection in Duchenne type muscular dystrophy using a new automatic techniqueJournal of Neurology, Neurosurgery & Psychiatry, 1972
- Histochemically demonstrable fibre abnormalities in normal skeletal muscle and in muscle from carriers of Duchenne muscular dystrophyJournal of Neurology, Neurosurgery & Psychiatry, 1971
- An assessment of the creatine kinase test in the detection of carriers of Duchenne muscular dystrophyThe Journal of Pediatrics, 1967
- Enzymaktivitätsbestimmungen bei Dystrophia musculorum progressivaKlinische Wochenschrift, 1966