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Physiologia Plantarum|December 30, 2017
Direct analysis by time-of-flight secondary ion mass spectrometry reveals action of bacterial laccase-mediator systems on both hardwood and softwood samplesRobyn E Goacher, Erick J Braham, Courtney L Michienzi, et al.Human Genetics|May 14, 1999
Skewed X-inactivation in a manifesting carrier of X-linked myotubular myopathy and in her non-manifesting carrier motherS M Tanner, K H Orstavik, M Kristiansen, et al.European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|October 24, 2007
A defect in the thymidine kinase 2 gene causing isolated mitochondrial myopathy without mtDNA depletionE Leshinsky-Silver, M Michelson, S Cohen, et al.Journal of Medical Genetics|May 1, 1997
Homozygosity by descent for a rare mutation in the myophosphorylase gene is associated with variable phenotypes in a Druze family with McArdle diseaseS Iyengar, H Kalinsky, S Weiss, et al.Journal of the Neurological Sciences|March 4, 1999
Subacute painful lumbosacral polyradiculoneuropathy in immunocompromised patientsI Steiner, O Cohen, R R Leker, et al.Annals of Neurology|April 1, 1997
Various types of hereditary inclusion body myopathies map to chromosome 9p1-q1Z Argov, E Tiram, I Eisenberg, et al.European Journal of Human Genetics : EJHG|July 21, 2001
Physical and transcriptional map of the hereditary inclusion body myopathy locus on chromosome 9p12-p13I Eisenberg, H Hochner, M Shemesh, et al.Genomics|January 16, 1999
Fine-structure mapping of the hereditary inclusion body myopathy locusI Eisenberg, C Thiel, T Levi, et al.Neuromuscular Disorders : NMD|September 11, 2007
Dysferlinopathy in the Jews of the Caucasus: a frequent mutation in the dysferlin geneE Leshinsky-Silver, Z Argov, L Rozenboim, et al.Neuromuscular Disorders : NMD|December 10, 1997
Epidemiology and inheritance of oculopharyngeal muscular dystrophy in IsraelS C Blumen, P Nisipeanu, M Sadeh, et al.Pageof 14