Genetic counselling in X-linked muscular dystrophy
- 30 June 1969
- journal article
- Published by Elsevier in Journal of the Neurological Sciences
- Vol. 8 (3), 579-587
- https://doi.org/10.1016/0022-510x(69)90016-1
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- The rationale of genetic counselingThe Journal of Pediatrics, 1968
- Detection of carriers of benign X-linked muscular dystrophy.BMJ, 1967
- Studies of the carrier state in the Duchenne type of muscular dystrophy. I. Effect of exercise on serum creatine kinase activity.Journal of Neurology, Neurosurgery & Psychiatry, 1967
- An assessment of the creatine kinase test in the detection of carriers of Duchenne muscular dystrophyThe Journal of Pediatrics, 1967
- Detection of subclinical and carrier states in Duchenne muscular dystrophyThe Journal of Pediatrics, 1966
- Genetic linkage between the loci for colour blindness and Duchenne type muscular dystrophy.Journal of Medical Genetics, 1966
- Alpha-hydroxybutyrate dehydrogenase activity in sex-linked muscular dystrophyJournal of Clinical Pathology, 1966
- Progressive Muskeldystrophie VII. Die Erfassung von Heterozygoten der Duchenne-Muskeldystrophie durch Messung der Serum-Kreatin-Kinase unter lokalisierter Arbeitsbelastung in AnoxieKlinische Wochenschrift, 1965
- Muscle Histology in Carriers of Duchenne Muscular DystrophyJournal of Medical Genetics, 1965
- REFRACTORY PERIOD OF MUSCLE AND ELECTROMYOGRAPHIC FINDINGS IN RELATIVES OF PATIENTS WITH MUSCULAR DYSTROPHYBrain, 1965