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E Nelis

Showing results (21-30 of 47) with videos related to

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Annals of Neurology|June 1, 1994
Deletion in the CMT1A locus on chromosome 17p11.2 in hereditary neuropathy with liability to pressure palsiesD Verhalle, A Löfgren, E Nelis, et al.
Neuroscience Letters|July 14, 1995
Molecular analysis of three cases with hereditary motor and sensory neuropathy with myelin outfoldingR James, E Bellone, E Nelis, et al.
Archives of Neurology|October 16, 1999
A novel type of hereditary motor and sensory neuropathy characterized by a mild phenotypeP De Jonghe, V Timmerman, E Nelis, et al.
Annals of Neurology|February 28, 2001
Further evidence that neurofilament light chain gene mutations can cause Charcot-Marie-Tooth disease type 2EP De Jonghe, I Mersivanova, E Nelis, et al.
Human Genetics|December 1, 1994
Rapid screening of myelin genes in CMT1 patients by SSCP analysis: identification of new mutations and polymorphisms in the P0 geneE Nelis, V Timmerman, P De Jonghe, et al.
Human Mutation|January 1, 1995
Mutations in the myelin protein zero gene associated with Charcot-Marie-Tooth disease type 1BP Latour, F Blanquet, E Nelis, et al.
American Journal of Human Genetics|June 1, 1994
Detection of tandem duplications and implications for linkage analysisT C Matise, A Chakravarti, P I Patel, et al.
Neurology|May 1, 1996
Linkage and mutation analysis of Charcot-Marie-Tooth neuropathy type 2 families with chromosomes 1p35-p36 and Xq13V Timmerman, P De Jonghe, P Spoelders, et al.
Human Molecular Genetics|July 1, 1996
Distal hereditary motor neuropathy type II (distal HMN II): mapping of a locus to chromosome 12q24V Timmerman, P De Jonghe, S Simokovic, et al.
Human Molecular Genetics|December 1, 1993
Origin of the de novo duplication in Charcot-Marie-Tooth disease type 1A: unequal nonsister chromatid exchange during spermatogenesisF Palau, A Löfgren, P De Jonghe, et al.
Pageof 5

Showing results (21-30 of 47) with videos related to

Sort By:
Pageof 5
Annals of Neurology|June 1, 1994
Deletion in the CMT1A locus on chromosome 17p11.2 in hereditary neuropathy with liability to pressure palsiesD Verhalle, A Löfgren, E Nelis, et al.
Neuroscience Letters|July 14, 1995
Molecular analysis of three cases with hereditary motor and sensory neuropathy with myelin outfoldingR James, E Bellone, E Nelis, et al.
Archives of Neurology|October 16, 1999
A novel type of hereditary motor and sensory neuropathy characterized by a mild phenotypeP De Jonghe, V Timmerman, E Nelis, et al.
Annals of Neurology|February 28, 2001
Further evidence that neurofilament light chain gene mutations can cause Charcot-Marie-Tooth disease type 2EP De Jonghe, I Mersivanova, E Nelis, et al.
Human Genetics|December 1, 1994
Rapid screening of myelin genes in CMT1 patients by SSCP analysis: identification of new mutations and polymorphisms in the P0 geneE Nelis, V Timmerman, P De Jonghe, et al.
Human Mutation|January 1, 1995
Mutations in the myelin protein zero gene associated with Charcot-Marie-Tooth disease type 1BP Latour, F Blanquet, E Nelis, et al.
American Journal of Human Genetics|June 1, 1994
Detection of tandem duplications and implications for linkage analysisT C Matise, A Chakravarti, P I Patel, et al.
Neurology|May 1, 1996
Linkage and mutation analysis of Charcot-Marie-Tooth neuropathy type 2 families with chromosomes 1p35-p36 and Xq13V Timmerman, P De Jonghe, P Spoelders, et al.
Human Molecular Genetics|July 1, 1996
Distal hereditary motor neuropathy type II (distal HMN II): mapping of a locus to chromosome 12q24V Timmerman, P De Jonghe, S Simokovic, et al.
Human Molecular Genetics|December 1, 1993
Origin of the de novo duplication in Charcot-Marie-Tooth disease type 1A: unequal nonsister chromatid exchange during spermatogenesisF Palau, A Löfgren, P De Jonghe, et al.
Pageof 5