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Human Mutation|February 5, 2000
New mutations in XNP/ATR-X gene: a further contribution to genotype/phenotype relationship in ATR/X syndrome. Mutations in brief no. 176. OnlineM Fichera, C Romano, L Castiglia, et al.Human Molecular Genetics|April 18, 1998
Correlation between varying levels of PMP22 expression and the degree of demyelination and reduction in nerve conduction velocity in transgenic miceC Huxley, E Passage, A M Robertson, et al.Brain : a Journal of Neurology|September 24, 2002
PMP22 overexpression causes dysmyelination in miceA Robaglia-Schlupp, J Pizant, J-C Norreel, et al.Journal of Medical Genetics|April 16, 1999
Evaluation of a mutation screening strategy for sporadic cases of ATR-X syndromeL Villard, M C Bonino, F Abidi, et al.Pageof 2