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British Medical Bulletin|January 28, 2024
Genetics in Parkinson's disease, state-of-the-art and future perspectivesL Trevisan, A Gaudio, E Monfrini, et al.American Journal of Medical Genetics|November 1, 1993
Parental origin of chromosome 4p deletion in Wolf-Hirschhorn syndromeB Dallapiccola, P Mandich, E Bellone, et al.American Journal of Medical Genetics|September 1, 1991
Non-random association between DNA markers and Huntington disease locus in the Italian populationA Novelletto, P Mandich, E Bellone, et al.Genomics|July 1, 1994
Mapping of the human NMDAR2B receptor subunit gene (GRIN2B) to chromosome 12p12P Mandich, A M Schito, E Bellone, et al.Neuroscience Letters|July 26, 1996
Use of cosH1 probe in hereditary neuropathy with liability to pressure palsies: a reliable genetic test for demonstration of identical size of 17p11.2 deletion in unrelated patientsE Bellone, A Schenone, G Mancardi, et al.Human Mutation|September 30, 1999
A novel mutation (D305V) in the early growth response 2 gene is associated with severe Charcot-Marie-Tooth type 1 diseaseE Bellone, E Di Maria, S Soriani, et al.Journal of Neurology, Neurosurgery, and Psychiatry|October 4, 2005
An abnormal mRNA produced by a novel PMP22 splice site mutation associated with HNPPE Bellone, P Balestra, G Ribizzi, et al.Neurology|November 1, 1992
HMSN III phenotype due to homozygous expression of a dominant HMSN II geneA Sghirlanzoni, D Pareyson, M R Balestrini, et al.Journal of Neurology, Neurosurgery, and Psychiatry|January 27, 2004
A novel mutation of myelin protein zero associated with an axonal form of Charcot-Marie-Tooth diseaseL Santoro, F Manganelli, E Di Maria, et al.Italian Journal of Neurological Sciences|February 1, 1994
Homozygous hypertrophic hereditary motor and sensory neuropathiesA Sghirlanzoni, D Pareyson, R Marazzi, et al.Pageof 6