Author:
Chabrol B.,Carrelet P.,Bollini G.
Reference19 articles.
1. Bingham PM, Shen N, Rennert H, Rorke LB, Black AW, Padilla M, Nordgren RE (1997) Artrhogryposis due to infantile neuronal degeneration associated with deletion of the SMNT gene. Neurology 49:848–851
2. Burglen L, Amiel J, Viollet L et al (1996) Survival motor neuron gene deletions in the arthrogryposis multiplex congenital spinal muscular atrophy association. J Clin Invest 98:1130–1132
3. Hall JG (1997) Arthrogryposis multiplex congenita: etiology, genetics, classification, diagnostic approach and general aspects J Pediatr Orthop B 6:159–166
4. Routon MC (1998) Myopathies congénitales. Dystrophies musculaires congénitales. In: Arthuis M, Dulac O, Mancini J, Pinsard N, Ponsot G (eds) Neurologie Pédiatrique. Flammarion Medecine-Sciences, Paris, pp 802–816
5. Dubowitz (1978) Muscle disorder in childood. Major problems in clinical pediatrics. Vol XVI, Saunders
Cited by
1 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献