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European Journal of Human Genetics : EJHG|January 1, 1996
Evidence for a common origin of most Friedreich ataxia chromosomes in the Spanish populationE Monrós, J Cañizares, M D Moltó, et al.Human Molecular Genetics|February 28, 1998
Fine mapping of de novo CMT1A and HNPP rearrangements within CMT1A-REPs evidences two distinct sex-dependent mechanisms and candidate sequences involved in recombinationJ Lopes, N Ravisé, A Vandenberghe, et al.Human Genetics|June 1, 1997
Mutational analysis of the MPZ, PMP22 and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsiesS Bort, E Nelis, V Timmerman, et al.Human Genetics|September 12, 2000
Genotype and phenotype analysis of Friedreich's ataxia compound heterozygous patientsM De Castro, J García-Planells, E Monrós, et al.Gut|June 19, 2014
The HLA-DQ2 genotype selects for early intestinal microbiota composition in infants at high risk of developing coeliac diseaseM Olivares, A Neef, G Castillejo, et al.Current Issues in Molecular Biology|May 30, 2009
Interplay between human leukocyte antigen genes and the microbial colonization process of the newborn intestineG De Palma, A Capilla, I Nadal, et al.Neurology|December 25, 2002
Mutations in GDAP1: autosomal recessive CMT with demyelination and axonopathyE Nelis, S Erdem, P Y K Van Den Bergh, et al.European Journal of Human Genetics : EJHG|January 1, 1996
Estimation of the mutation frequencies in Charcot-Marie-Tooth disease type 1 and hereditary neuropathy with liability to pressure palsies: a European collaborative studyE Nelis, C Van Broeckhoven, P De Jonghe, et al.Science (New York, N.Y.)|March 8, 1996
Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansionV Campuzano, L Montermini, M D Moltò, et al.Pageof 6