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Journal of Neurology|May 1, 1996
Sensory involvement in X-linked spino-bulbar muscular atrophy (Kennedy's syndrome): an electrophysiological studyA Polo, F Teatini, S D'Anna, et al.Journal of Endocrinological Investigation|May 1, 1994
Male hypogonadism in myotonic dystrophy is related to (CTG)n triplet mutationI Mastrogiacomo, E Pagani, G Novelli, et al.Biochemical and Biophysical Research Communications|November 30, 1993
Human elongation factor EF-1 beta: cloning and characterization of the EF1 beta 5a gene and assignment of EF-1 beta isoforms to chromosomes 2,5,15 and XA Pizzuti, M Gennarelli, G Novelli, et al.Human Genetics|October 1, 1995
Analysis of the elastin gene in 60 patients with clinical diagnosis of Williams syndromeA Mari, F Amati, R Mingarelli, et al.Biochemical and Biophysical Research Communications|August 4, 1995
Survival motor neuron gene transcript analysis in muscles from spinal muscular atrophy patientsM Gennarelli, M Lucarelli, F Capon, et al.Journal of Applied Microbiology|May 24, 2011
Isolation and phenotypic characterization of Lactobacillus casei and Lactobacillus paracasei bacteriophage-resistant mutantsM L Capra, D J Mercanti, L C Rossetti, et al.Journal of Applied Microbiology|June 3, 2009
Diversity among Lactobacillus paracasei phages isolated from a probiotic dairy product plantM L Capra, A G Binetti, D J Mercanti, et al.Journal of Craniofacial Genetics and Developmental Biology|April 1, 1996
The search for hemizygosity at 22qll in patients with isolated cleft palateR Mingarelli, M C Digilio, A Mari, et al.Clinical Genetics|June 18, 2004
High frequency of subtelomeric rearrangements in a cohort of 92 patients with severe mental retardation and dysmorphismA Novelli, C Ceccarini, L Bernardini, et al.Molecular and Cellular Probes|August 11, 1999
Diagnosis of DiGeorge and Williams syndromes using FISH analysis of peripheral blood smearsA Novelli, M Sabani, A Caiola, et al.Pageof 34