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European Neurology|September 4, 1999
Classical Friedreich's ataxia and its genotypeJ Martin, L Martin, A Löfgren, et al.Medicina Clinica|May 5, 1990
[Genetic analysis of Friedreich's ataxia using polymorphic DNA markers]F Palau, J J Vílchez, M Beneyto, et al.Clinical Genetics|May 2, 2007
The p.R1109X mutation in SH3TC2 gene is predominant in Spanish Gypsies with Charcot-Marie-Tooth disease type 4R Claramunt, T Sevilla, V Lupo, et al.Human Molecular Genetics|November 5, 1999
Homologous DNA exchanges in humans can be explained by the yeast double-strand break repair model: a study of 17p11.2 rearrangements associated with CMT1A and HNPPJ Lopes, S Tardieu, K Silander, et al.Acta Neurochirurgica|October 4, 2024
MGMT methylation and its prognostic significance in inoperable IDH-wildtype glioblastoma: the MGMT-GBM studyPrajwal Ghimire, Ahmad Kamaludin, Berta F Palau, et al.Neuromuscular Disorders : NMD|June 1, 2014
A novel locus for a hereditary recurrent neuropathy on chromosome 21q21E Calpena, D Martínez-Rubio, J Arpa, et al.Allergologia Et Immunopathologia|May 1, 1985
Mechanism of suppression of the depressed lymphocyte response in lung cancer patientsV Alberola, A González-Molina, A Trenor, et al.Muscle & Nerve|August 9, 2001
Diagnostic strategy for familial and sporadic cases of neuropathy associated with 17p11.2 deletionJ Infante, A García, O Combarros, et al.Clinical Genetics|September 18, 2012
Genetics of the Charcot-Marie-Tooth disease in the Spanish Gypsy population: the hereditary motor and sensory neuropathy-Russe in depthT Sevilla, D Martínez-Rubio, C Márquez, et al.Journal of Medical Genetics|September 1, 1995
Influence of the sex of the transmitting grandparent in congenital myotonic dystrophyA López de Munain, A M Cobo, J J Poza, et al.Pageof 6