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Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|February 13, 2004
Molecular bases of autosomal recessive limb-girdle muscular dystrophiesV Nigro
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|October 17, 2006
Readthrough strategies for stop codons in Duchenne muscular dystrophyS Aurino, V Nigro
Journal of Medical Genetics|June 1, 1977
Bilateral absence of the kidneys and ureters. Three cases reported in one familyH M Pashayan, T Dowd, A V Nigro
Neuromuscular Disorders : NMD|July 1, 1994
Mutation of dystrophin gene and cardiomyopathyG Nigro, L Politano, V Nigro, et al.
Journal of Dental Research|February 19, 2015
Genetic association of ARHGAP21 gene variant with mandibular prognathismL Perillo, A MonsurrĂ², E Bonci, et al.
Genomics|November 5, 1997
Exon-intron organization of the human dystrophin geneC Nobile, J Marchi, V Nigro, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|June 25, 2016
A Steady-State Head-to-Head Pharmacokinetic Comparison of All FK-506 (Tacrolimus) Formulations (ASTCOFF): An Open-Label, Prospective, Randomized, Two-Arm, Three-Period Crossover StudyS Tremblay, V Nigro, J Weinberg, et al.
FEBS Letters|February 17, 1997
The fourth component of the sarcoglycan complexM Yoshida, S Noguchi, E Wakabayashi, et al.
Biochemical and Biophysical Research Communications|April 30, 1985
Particulate nature of the unoccupied uterine estrogen receptorA M Molinari, N Medici, I Armetta, et al.
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