The myopathic variety of arthrogryposis multiplex congenita: A disorder with autosomal recessive inheritance
- 1 July 1972
- journal article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 81 (1) , 76-82
- https://doi.org/10.1016/s0022-3476(72)80377-9
Abstract
No abstract availableThis publication has 18 references indexed in Scilit:
- The myopathology of the Prune Belly SyndromeJournal of the Neurological Sciences, 1972
- Arthrogryposis multiplex congenita: A clinical investigationThe Journal of Pediatrics, 1970
- Pathology of muscular hypotonia in the Prader-Willi syndrome: Light and electron microscopic studyJournal of the Neurological Sciences, 1969
- Arthrogryposis accompanying congenital spinal-type muscular atrophy.Archives of Disease in Childhood, 1967
- CHANGES IN MUSCLE STRUCTURE IN DYSTROPHIC PATIENTS, CARRIERS AND NORMAL SIBLINGS SEEN BY ELECTRON MICROSCOPY; CORRELATION WITH LEVELS OF SERUM CREATINEPHOSPHOKINASE (CPK)*Annals of the New York Academy of Sciences, 1966
- ARTHROGRYPOSIS MULTIPLEX DUE TO CONGENITAL MUSCULAR DYSTROPHYBrain, 1957
- Arthrogryposis multiplex congenita: Case reportThe Journal of Pediatrics, 1956
- ARTHROGRYPOSIS MULTIPLEX CONGENITAArchives of Surgery, 1943
- Amyoplasia Congenita: (Multiple congenital articular rigidity: Arthrogryposis multiplex congenita)Archives of Disease in Childhood, 1932
- ARTHROGRYPOSIS MULTIPLEX CONGENITAPublished by American Medical Association (AMA) ,1923