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V Timmerman

Showing results (51-60 of 105) with videos related to

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Journal of the Peripheral Nervous System : JPNS|August 12, 1999
Novel PCR-based diagnostic tools for Charcot-Marie-Tooth type 1A and hereditary neuropathy with liability to pressure palsiesE A Stronach, C Clark, C Bell, et al.
Annals of Human Genetics|March 24, 1999
Mutation analysis of a putative sialyltransferase gene, the SFRS2 splicing factor gene and the c-myb ET-locus in two families with hereditary neuralgic amyotrophy (HNA)G Kuhlenbaeumer, J Meuleman, A Schirmacher, 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.
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.
Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 1996
Hereditary neuropathy with liability to pressure palsies with a partial deletion of the region often duplicated in Charcot-Marie-Tooth disease, type 1AF Chapon, P Diraison, B Lechevalier, 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.
Pathology, Research and Practice|April 21, 2001
Infantile demyelinating neuropathy associated with a de novo point mutation on Ser72 in PMP22 and basal lamina onion bulbs in skin biopsyC Ceuterick-de Groote, P De Jonghe, V Timmerman, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Mutation screening of Charcot-Marie-Tooth patients in PolandA Kochański, V Timmerman, H Jedrzejowska, et al.
Annals of the New York Academy of Sciences|November 1, 2017
Mutation Screening of Charcot-Marie-Tooth Patients in PolandA Kochański, V Timmerman, H Jedrzejowska, et al.
Pageof 11

Showing results (51-60 of 105) with videos related to

Sort By:
Pageof 11
Journal of the Peripheral Nervous System : JPNS|August 12, 1999
Novel PCR-based diagnostic tools for Charcot-Marie-Tooth type 1A and hereditary neuropathy with liability to pressure palsiesE A Stronach, C Clark, C Bell, et al.
Annals of Human Genetics|March 24, 1999
Mutation analysis of a putative sialyltransferase gene, the SFRS2 splicing factor gene and the c-myb ET-locus in two families with hereditary neuralgic amyotrophy (HNA)G Kuhlenbaeumer, J Meuleman, A Schirmacher, 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.
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.
Journal of Neurology, Neurosurgery, and Psychiatry|November 1, 1996
Hereditary neuropathy with liability to pressure palsies with a partial deletion of the region often duplicated in Charcot-Marie-Tooth disease, type 1AF Chapon, P Diraison, B Lechevalier, 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.
Pathology, Research and Practice|April 21, 2001
Infantile demyelinating neuropathy associated with a de novo point mutation on Ser72 in PMP22 and basal lamina onion bulbs in skin biopsyC Ceuterick-de Groote, P De Jonghe, V Timmerman, et al.
Annals of the New York Academy of Sciences|December 10, 1999
Mutation screening of Charcot-Marie-Tooth patients in PolandA Kochański, V Timmerman, H Jedrzejowska, et al.
Annals of the New York Academy of Sciences|November 1, 2017
Mutation Screening of Charcot-Marie-Tooth Patients in PolandA Kochański, V Timmerman, H Jedrzejowska, et al.
Pageof 11