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E Nelis

Showing results (1-10 of 47) with videos related to

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Human Mutation|January 15, 1999
Mutations in the peripheral myelin genes and associated genes in inherited peripheral neuropathiesE Nelis, N Haites, C Van Broeckhoven
Acta Neurologica Belgica|December 1, 2000
Molecular genetics of inherited peripheral neuropathies: who are the actors?J Meuleman, V Timmerman, E Nelis, et al.
Journal of Medical Genetics|June 1, 1994
Charcot-Marie-Tooth disease in northern Sweden: pedigree analysis and the presence of the duplication in chromosome 17p11.2B H Holmberg, G Holmgren, E Nelis, et al.
Neurogenetics|December 14, 1999
Molecular genetics and biology of inherited peripheral neuropathies: a fast-moving fieldE Nelis, V Timmerman, P De Jonghe, et al.
Neurology|June 1, 1997
Further evidence supporting linkage of hereditary neuralgic amyotrophy to chromosome 17qM Wehnert, V Timmerman, P Spoelders, et al.
Journal of the Peripheral Nervous System : JPNS|January 1, 1997
Charcot-Marie-Tooth disease and related peripheral neuropathiesP De Jonghe, V Timmerman, E Nelis, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 10, 1999
Central visual, acoustic, and motor pathway involvement in a Charcot-Marie-Tooth family with an Asn205Ser mutation in the connexin 32 geneM Bähr, F Andres, V Timmerman, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Molecular diagnostic testing in Charcot-Marie-Tooth disease and related disorders. Approaches and resultsP De Jonghe, E Nelis, V Timmerman, et al.
Journal of Medical Genetics|October 1, 1994
Linkage and mutation analysis in an extended family with Charcot-Marie-Tooth disease type 1BE Nelis, V Timmerman, P De Jonghe, et al.
Prenatal Diagnosis|July 1, 1995
Prenatal diagnosis of Charcot-Marie-Tooth disease type 1A (CMT1A) using molecular genetic techniquesR Navon, V Timmerman, A Löfgren, et al.
Pageof 5

Showing results (1-10 of 47) with videos related to

Sort By:
Pageof 5
Human Mutation|January 15, 1999
Mutations in the peripheral myelin genes and associated genes in inherited peripheral neuropathiesE Nelis, N Haites, C Van Broeckhoven
Acta Neurologica Belgica|December 1, 2000
Molecular genetics of inherited peripheral neuropathies: who are the actors?J Meuleman, V Timmerman, E Nelis, et al.
Journal of Medical Genetics|June 1, 1994
Charcot-Marie-Tooth disease in northern Sweden: pedigree analysis and the presence of the duplication in chromosome 17p11.2B H Holmberg, G Holmgren, E Nelis, et al.
Neurogenetics|December 14, 1999
Molecular genetics and biology of inherited peripheral neuropathies: a fast-moving fieldE Nelis, V Timmerman, P De Jonghe, et al.
Neurology|June 1, 1997
Further evidence supporting linkage of hereditary neuralgic amyotrophy to chromosome 17qM Wehnert, V Timmerman, P Spoelders, et al.
Journal of the Peripheral Nervous System : JPNS|January 1, 1997
Charcot-Marie-Tooth disease and related peripheral neuropathiesP De Jonghe, V Timmerman, E Nelis, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 10, 1999
Central visual, acoustic, and motor pathway involvement in a Charcot-Marie-Tooth family with an Asn205Ser mutation in the connexin 32 geneM Bähr, F Andres, V Timmerman, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Molecular diagnostic testing in Charcot-Marie-Tooth disease and related disorders. Approaches and resultsP De Jonghe, E Nelis, V Timmerman, et al.
Journal of Medical Genetics|October 1, 1994
Linkage and mutation analysis in an extended family with Charcot-Marie-Tooth disease type 1BE Nelis, V Timmerman, P De Jonghe, et al.
Prenatal Diagnosis|July 1, 1995
Prenatal diagnosis of Charcot-Marie-Tooth disease type 1A (CMT1A) using molecular genetic techniquesR Navon, V Timmerman, A Löfgren, et al.
Pageof 5