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Journal of the Neurological Sciences|May 1, 1996
Molecular genetics of familial spastic paraplegia: a multitude of responsible genesH Kobayashi, C A Garcia, G Alfonso, et al.Neuromuscular Disorders : NMD|May 1, 1995
Phospholipase A2 activity in dystrophinopathiesM Lindahl, E Bäckman, K G Henriksson, et al.Developmental Dynamics : an Official Publication of the American Association of Anatomists|March 7, 1998
Role of the nerve in determining fetal skeletal muscle phenotypeC H Washabaugh, M P Ontell, Z Shan, et al.Human Molecular Genetics|July 1, 1995
A gene for a severe lethal form of X-linked arthrogryposis (X-linked infantile spinal muscular atrophy) maps to human chromosome Xp11.3-q11.2H Kobayashi, L Baumbach, T C Matise, et al.Neuropediatrics|June 21, 2002
Alpha-sarcoglycan deficiency featuring exercise intolerance and myoglobinuriaT Mongini, C Doriguzzi, I Bosone, et al.Mental Retardation and Developmental Disabilities Research Reviews|July 12, 2002
Associations between MeCP2 mutations, X-chromosome inactivation, and phenotypeK C Hoffbuhr, L M Moses, M A Jerdonek, et al.Gene Therapy|May 26, 1999
rAAV vector-mediated sarcogylcan gene transfer in a hamster model for limb girdle muscular dystrophyJ Li, D Dressman, Y P Tsao, et al.The Journal of Clinical Endocrinology and Metabolism|July 1, 1997
Evidence for a heterozygote advantage in congenital adrenal hyperplasia due to 21-hydroxylase deficiencyS F Witchel, P A Lee, M Suda-Hartman, et al.Journal of the Neurological Sciences|March 1, 1994
A role for mast cells in the progression of Duchenne muscular dystrophy? Correlations in dystrophin-deficient humans, dogs, and miceJ R Gorospe, M D Tharp, J Hinckley, et al.American Journal of Human Genetics|July 1, 1997
Familial skewed X inactivation: a molecular trait associated with high spontaneous-abortion rate maps to Xq28E Pegoraro, J Whitaker, P Mowery-Rushton, et al.Pageof 19