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E Nelis

Showing results (11-20 of 47) with videos related to

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Annals of the New York Academy of Sciences|November 1, 2017
Molecular Diagnostic Testing in Charcot-Marie-Tooth Disease and Related Disorders: Approaches and ResultsP De Jonghe, E Nelis, V Timmerman, et al.
Annals of Human Genetics|February 20, 2002
Exclusion of 5 functional candidate genes for distal hereditary motor neuropathy type II (distal HMN II) linked to 12q24.3J Irobi, E Nelis, J Meuleman, et al.
Genetic Analysis : Biomolecular Engineering|December 3, 1998
An adhesion test system based on Schneider cells to determine genotype-phenotype correlations for mutated P0 proteinsA B Ekici, C Fuchs, E Nelis, et al.
Human Mutation|January 1, 1996
A de novo duplication in 17p11.2 and a novel mutation in the Po gene in two Déjérine-Sottas syndrome patientsK Silander, P Meretoja, E Nelis, et al.
Annals of Human Genetics|January 25, 2008
Charcot-Marie-Tooth disease: a clinico-genetic confrontationN Barisic, K G Claeys, M Sirotković-Skerlev, et al.
American Journal of Human Genetics|May 23, 1998
Human meiotic recombination products revealed by sequencing a hotspot for homologous strand exchange in multiple HNPP deletion patientsL T Reiter, P J Hastings, E Nelis, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Comparison of single-strand conformation polymorphism and heteroduplex analysis for detection of mutations in Charcot-Marie-Tooth type 1 disease and related peripheral neuropathiesE Nelis, L E Warner, E D Vriendt, et al.
Journal of Medical Genetics|July 25, 1998
Mutation analysis of the nerve specific promoter of the peripheral myelin protein 22 gene in CMT1 disease and HNPPE Nelis, P De Jonghe, E De Vriendt, et al.
Journal of Medical Genetics|January 1, 1992
Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). HMSN Collaborative Research GroupP Raeymaekers, V Timmerman, E Nelis, et al.
Journal of the Neurological Sciences|May 1, 1992
Linkage analysis of distal hereditary motor neuropathy type II (distal HMN II) in a single pedigreeV Timmerman, P Raeymaekers, E Nelis, et al.
Pageof 5

Showing results (11-20 of 47) with videos related to

Sort By:
Pageof 5
Annals of the New York Academy of Sciences|November 1, 2017
Molecular Diagnostic Testing in Charcot-Marie-Tooth Disease and Related Disorders: Approaches and ResultsP De Jonghe, E Nelis, V Timmerman, et al.
Annals of Human Genetics|February 20, 2002
Exclusion of 5 functional candidate genes for distal hereditary motor neuropathy type II (distal HMN II) linked to 12q24.3J Irobi, E Nelis, J Meuleman, et al.
Genetic Analysis : Biomolecular Engineering|December 3, 1998
An adhesion test system based on Schneider cells to determine genotype-phenotype correlations for mutated P0 proteinsA B Ekici, C Fuchs, E Nelis, et al.
Human Mutation|January 1, 1996
A de novo duplication in 17p11.2 and a novel mutation in the Po gene in two Déjérine-Sottas syndrome patientsK Silander, P Meretoja, E Nelis, et al.
Annals of Human Genetics|January 25, 2008
Charcot-Marie-Tooth disease: a clinico-genetic confrontationN Barisic, K G Claeys, M Sirotković-Skerlev, et al.
American Journal of Human Genetics|May 23, 1998
Human meiotic recombination products revealed by sequencing a hotspot for homologous strand exchange in multiple HNPP deletion patientsL T Reiter, P J Hastings, E Nelis, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Comparison of single-strand conformation polymorphism and heteroduplex analysis for detection of mutations in Charcot-Marie-Tooth type 1 disease and related peripheral neuropathiesE Nelis, L E Warner, E D Vriendt, et al.
Journal of Medical Genetics|July 25, 1998
Mutation analysis of the nerve specific promoter of the peripheral myelin protein 22 gene in CMT1 disease and HNPPE Nelis, P De Jonghe, E De Vriendt, et al.
Journal of Medical Genetics|January 1, 1992
Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). HMSN Collaborative Research GroupP Raeymaekers, V Timmerman, E Nelis, et al.
Journal of the Neurological Sciences|May 1, 1992
Linkage analysis of distal hereditary motor neuropathy type II (distal HMN II) in a single pedigreeV Timmerman, P Raeymaekers, E Nelis, et al.
Pageof 5